Linked Data
ClinVar Variation Id:
237524
dbSNP Id:
rs753245823
ExAC:
17:29552133 T / C
gnomAD v2:
17-29552133-T-C
gnomAD v4:
17-31225115-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31225115T>C , CM000679.2:g.31225115T>C | GRCh38 |
| NC_000017.10:g.29552133T>C , CM000679.1:g.29552133T>C | GRCh37 |
| NC_000017.9:g.26576259T>C | NCBI36 |
| NG_009018.1:g.135139T>C , LRG_214:g.135139T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.1911T>C | ENSP00000512431.1:p.Cys637= | |
| ENST00000691014.1:c.1896T>C | ENSP00000510595.1:p.Cys632= | |
| ENST00000358273.9:c.1866T>C MANE Select | ENSP00000351015.4:p.Cys622= | |
| ENST00000356175.7:c.1866T>C | ENSP00000348498.3:p.Cys622= | |
| ENST00000358273.8:c.1866T>C | ENSP00000351015.4:p.Cys622= | |
| ENST00000456735.6:c.864T>C | ENSP00000389907.2:p.Cys288= | |
| ENST00000493220.5:n.33T>C | ||
| ENST00000495910.6:c.1641T>C | ||
| ENST00000579081.5:c.1968T>C | ENSP00000462408.1:p.Cys656= | |
| NM_000267.3:c.1866T>C , LRG_214t1:c.1866T>C | NP_000258.1:p.Cys622= | |
| NM_001042492.2:c.1866T>C , LRG_214t2:c.1866T>C | NP_001035957.1:p.Cys622= | |
| XM_005257983.1:c.1866T>C | XP_005258040.1:p.Cys622= | |
| XM_005257984.1:c.1866T>C | XP_005258041.1:p.Cys622= | |
| XM_006721922.1:c.1896T>C | XP_006721985.1:p.Cys632= | |
| XM_006721923.2:c.1857T>C | XP_006721986.1:p.Cys619= | |
| XM_006721924.1:c.1896T>C | XP_006721987.1:p.Cys632= | |
| XM_006721925.1:c.1896T>C | XP_006721988.1:p.Cys632= | |
| XM_006721926.2:c.1896T>C | XP_006721989.1:p.Cys632= | |
| XM_006721927.1:c.1896T>C | XP_006721990.1:p.Cys632= | |
| XM_006721928.2:c.1896T>C | XP_006721991.1:p.Cys632= | |
| XM_011524852.1:c.1893T>C | XP_011523154.1:p.Cys631= | |
| XM_011524853.1:c.1857T>C | XP_011523155.1:p.Cys619= | |
| XM_011524854.1:c.1857T>C | XP_011523156.1:p.Cys619= | |
| XM_011524855.1:c.1857T>C | XP_011523157.1:p.Cys619= | |
| XM_011524856.1:c.1857T>C | XP_011523158.1:p.Cys619= | |
| XM_011524857.1:c.1896T>C | XP_011523159.1:p.Cys632= | |
| NM_001042492.3:c.1866T>C MANE Select | NP_001035957.1:p.Cys622= |