Linked Data
ClinVar Variation Id:
179964
dbSNP Id:
rs727505247
ExAC:
11:17531094 G / A
gnomAD v2:
11-17531094-G-A
gnomAD v3:
11-17509547-G-A
gnomAD v4:
11-17509547-G-A
COSMIC:
COSM2091753
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17509547G>A , CM000673.2:g.17509547G>A | GRCh38 |
| NC_000011.9:g.17531094G>A , CM000673.1:g.17531094G>A | GRCh37 |
| NC_000011.8:g.17487670G>A | NCBI36 |
| NG_011883.1:g.39870C>T | |
| NG_011883.2:g.39870C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005226.12:c.1822C>T MANE Select | ENSP00000005226.7:p.Pro608Ser | |
| ENST00000318024.9:c.1285-7567C>T MANE Plus Clinical | ENSP00000317018.4:n.1285-7567C>T | |
| ENST00000005226.11:c.1822C>T | ENSP00000005226.7:p.Pro608Ser | |
| ENST00000318024.8:c.1285-7567C>T | ENSP00000317018.4:n.1285-7567C>T | |
| ENST00000526313.5:c.1211-7567C>T | ENSP00000432236.1:n.1211-7567C>T | |
| ENST00000527020.5:c.1228-7567C>T | ENSP00000436934.1:n.1228-7567C>T | |
| ENST00000527720.5:c.1192-7567C>T | ENSP00000432944.1:n.1192-7567C>T | |
| ENST00000529563.5:n.168+6908C>T | ||
| NM_001297764.1:c.1228-7567C>T | NP_001284693.1:n.1228-7567C>T | |
| NM_005709.3:c.1285-7567C>T | NP_005700.2:n.1285-7567C>T | |
| NM_153676.3:c.1822C>T | NP_710142.1:p.Pro608Ser | |
| NR_123738.1:n.1320-7567C>T | ||
| XM_011519831.1:c.1846C>T | XP_011518133.1:p.Pro616Ser | |
| XM_011519832.1:c.1437+2355C>T | XP_011518134.1:n.1437+2355C>T | |
| XM_011519833.1:c.1334+6694C>T | XP_011518135.1:n.1334+6694C>T | |
| XR_930841.1:n.1655+2355C>T | ||
| XR_930842.1:n.1596+2355C>T | ||
| XM_011519832.3:c.1437+2355C>T | XP_011518134.1:n.1437+2355C>T | |
| XM_017017072.1:c.1846C>T | XP_016872561.1:p.Pro616Ser | |
| XM_017017073.1:c.1789C>T | XP_016872562.1:p.Pro597Ser | |
| XM_017017074.1:c.1555-318C>T | XP_016872563.1:n.1555-318C>T | |
| XM_017017075.1:c.1822C>T | XP_016872564.1:p.Pro608Ser | |
| XR_001747717.2:n.1443+6694C>T | ||
| NM_153676.4:c.1822C>T MANE Select | NP_710142.1:p.Pro608Ser | |
| NM_001297764.2:c.1228-7567C>T | NP_001284693.1:n.1228-7567C>T | |
| NM_005709.4:c.1285-7567C>T MANE Plus Clinical | NP_005700.2:n.1285-7567C>T | |
| NR_123738.2:n.1320-7567C>T |