Linked Data
dbSNP Id:
rs7210438
gnomAD v2:
17-79060180-C-T
gnomAD v3:
17-81086380-C-T
gnomAD v4:
17-81086380-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.81086380C>T , CM000679.2:g.81086380C>T | GRCh38 |
| NC_000017.10:g.79060180C>T , CM000679.1:g.79060180C>T | GRCh37 |
| NC_000017.9:g.76674775C>T | NCBI36 |
| NG_029486.1:g.56234C>T | |
| NG_029486.2:g.56234C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000428708.7:c.352-63C>T MANE Select | ENSP00000401022.2:n.352-63C>T | |
| ENST00000321280.11:c.352-63C>T | ENSP00000315685.7:n.352-63C>T | |
| ENST00000321300.10:c.352-63C>T | ENSP00000316338.6:n.352-63C>T | |
| ENST00000428708.6:c.352-63C>T | ENSP00000401022.2:n.352-63C>T | |
| ENST00000435091.7:c.352-63C>T | ENSP00000413069.3:n.352-63C>T | |
| ENST00000571530.5:c.292-63C>T | ENSP00000458202.1:n.292-63C>T | |
| ENST00000572073.5:c.178-63C>T | ENSP00000459787.1:n.178-63C>T | |
| ENST00000572329.5:c.441-63C>T | ENSP00000460492.1:n.441-63C>T | |
| ENST00000572918.5:c.292-63C>T | ENSP00000460131.1:n.292-63C>T | |
| ENST00000573017.5:n.387-63C>T | ||
| ENST00000573659.5:c.178-63C>T | ENSP00000461736.1:n.178-63C>T | |
| ENST00000573677.5:c.178-63C>T | ENSP00000458735.1:n.178-63C>T | |
| ENST00000573894.5:n.431-63C>T | ||
| ENST00000574688.5:n.554-63C>T | ||
| ENST00000574804.5:c.168-63C>T | ENSP00000459730.1:n.168-63C>T | |
| ENST00000575245.5:c.451-63C>T | ENSP00000461144.1:n.451-63C>T | |
| ENST00000575712.5:c.352-63C>T | ENSP00000458964.1:n.352-63C>T | |
| ENST00000575750.5:c.*102-63C>T | ENSP00000460344.1:n.*102-63C>T | |
| ENST00000575958.5:c.178-63C>T | ENSP00000458522.1:n.178-63C>T | |
| ENST00000575989.5:c.178-63C>T | ENSP00000458494.1:n.178-63C>T | |
| ENST00000576225.5:n.632-63C>T | ||
| ENST00000576364.6:n.252-63C>T | ||
| ENST00000577097.5:n.478-63C>T | ||
| NM_001144888.1:c.352-63C>T | NP_001138360.1:n.352-63C>T | |
| NM_006340.2:c.352-63C>T | NP_006331.1:n.352-63C>T | |
| NM_017450.2:c.352-63C>T | NP_059344.1:n.352-63C>T | |
| NM_017451.2:c.352-63C>T | NP_059345.1:n.352-63C>T | |
| XM_005256943.1:c.451-63C>T | XP_005257000.1:n.451-63C>T | |
| XM_005256944.1:c.451-63C>T | XP_005257001.1:n.451-63C>T | |
| XM_005256945.1:c.451-63C>T | XP_005257002.1:n.451-63C>T | |
| XM_005256948.2:c.352-63C>T | XP_005257005.1:n.352-63C>T | |
| XM_006721635.1:c.451-63C>T | XP_006721698.1:n.451-63C>T | |
| XM_006721636.1:c.451-63C>T | XP_006721699.1:n.451-63C>T | |
| XM_006721637.1:c.352-63C>T | XP_006721700.1:n.352-63C>T | |
| XM_011524193.1:c.451-63C>T | XP_011522495.1:n.451-63C>T | |
| XM_011524194.1:c.451-63C>T | XP_011522496.1:n.451-63C>T | |
| XM_005256948.3:c.352-63C>T | XP_005257005.1:n.352-63C>T | |
| XM_006721637.2:c.352-63C>T | XP_006721700.1:n.352-63C>T | |
| XM_017024017.1:c.334-63C>T | XP_016879506.1:n.334-63C>T | |
| XM_017024018.1:c.118-63C>T | XP_016879507.1:n.118-63C>T | |
| XM_024450534.1:c.355-63C>T | XP_024306302.1:n.355-63C>T | |
| XM_024450535.1:c.118-63C>T | XP_024306303.1:n.118-63C>T | |
| NM_001144888.2:c.352-63C>T MANE Select | NP_001138360.1:n.352-63C>T | |
| NM_006340.3:c.352-63C>T | NP_006331.1:n.352-63C>T | |
| NM_017450.3:c.352-63C>T | NP_059344.1:n.352-63C>T | |
| NM_017451.3:c.352-63C>T | NP_059345.1:n.352-63C>T | |
| NM_001385127.1:c.352-63C>T | NP_001372056.1:n.352-63C>T | |
| NM_001385128.1:c.352-63C>T | NP_001372057.1:n.352-63C>T | |
| NM_001385129.1:c.451-63C>T | NP_001372058.1:n.451-63C>T | |
| NM_001385130.1:c.451-63C>T | NP_001372059.1:n.451-63C>T | |
| NM_001385131.1:c.352-63C>T | NP_001372060.1:n.352-63C>T | |
| NM_001385132.1:c.451-63C>T | NP_001372061.1:n.451-63C>T | |
| NM_001385133.1:c.451-63C>T | NP_001372062.1:n.451-63C>T | |
| NM_001385134.1:c.451-63C>T | NP_001372063.1:n.451-63C>T | |
| NM_001385135.1:c.451-63C>T | NP_001372064.1:n.451-63C>T | |
| NM_001385136.1:c.451-63C>T | NP_001372065.1:n.451-63C>T | |
| NM_001385137.1:c.427-63C>T | NP_001372066.1:n.427-63C>T | |
| NM_001385138.1:c.352-63C>T | NP_001372067.1:n.352-63C>T | |
| NM_001385139.1:c.352-63C>T | NP_001372068.1:n.352-63C>T | |
| NM_001385140.1:c.352-63C>T | NP_001372069.1:n.352-63C>T | |
| NM_001385141.1:c.352-63C>T | NP_001372070.1:n.352-63C>T | |
| NM_001385144.1:c.346-63C>T | NP_001372073.1:n.346-63C>T | |
| NM_001385145.1:c.352-63C>T | NP_001372074.1:n.352-63C>T | |
| NM_001385146.1:c.352-63C>T | NP_001372075.1:n.352-63C>T | |
| NM_001385147.1:c.178-63C>T | NP_001372076.1:n.178-63C>T | |
| NM_001385148.1:c.178-63C>T | NP_001372077.1:n.178-63C>T | |
| NM_001385149.1:c.178-63C>T | NP_001372078.1:n.178-63C>T | |
| NM_001385150.1:c.118-63C>T | NP_001372079.1:n.118-63C>T | |
| NM_001385151.1:c.118-63C>T | NP_001372080.1:n.118-63C>T | |
| NM_001385152.1:c.118-63C>T | NP_001372081.1:n.118-63C>T | |
| NM_001385153.1:c.118-63C>T | NP_001372082.1:n.118-63C>T | |
| NM_001385154.1:c.118-63C>T | NP_001372083.1:n.118-63C>T | |
| NM_001385155.1:c.118-63C>T | NP_001372084.1:n.118-63C>T | |
| NM_001385156.1:c.118-63C>T | NP_001372085.1:n.118-63C>T | |
| NM_001385158.1:c.-378-63C>T | NP_001372087.1:n.-378-63C>T | |
| NR_169574.1:n.456-63C>T | ||
| NR_169575.1:n.446-63C>T | ||
| NR_169576.1:n.545-63C>T | ||
| NR_169577.1:n.446-63C>T | ||
| NR_169578.1:n.456-63C>T | ||
| NR_169579.1:n.555-63C>T | ||
| NR_169580.1:n.273-63C>T |