Linked Data
ClinVar Variation Id:
36416
dbSNP Id:
rs193922362
ExAC:
19:17947957 G / A
gnomAD v2:
19-17947957-G-A
gnomAD v3:
19-17837148-G-A
gnomAD v4:
19-17837148-G-A
PubMed:
PMID:9354668
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17837148G>A , CM000681.2:g.17837148G>A | GRCh38 |
| NC_000019.9:g.17947957G>A , CM000681.1:g.17947957G>A | GRCh37 |
| NC_000019.8:g.17808957G>A | NCBI36 |
| NG_007273.1:g.15844C>T , LRG_77:g.15844C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000526008.6:c.*324C>T | ENSP00000513006.1:n.*324C>T | |
| ENST00000696967.1:n.944C>T | ||
| ENST00000696970.1:n.422C>T | ||
| ENST00000458235.7:c.1767C>T MANE Select | ENSP00000391676.1:p.Gly589= | |
| ENST00000458235.5:c.1767C>T | ENSP00000391676.1:p.Gly589= | |
| ENST00000527031.5:n.1857C>T | ||
| ENST00000527670.5:c.1767C>T | ENSP00000432511.1:p.Gly589= | |
| ENST00000534444.1:c.1767C>T | ENSP00000436421.1:p.Gly589= | |
| NM_000215.3:c.1767C>T , LRG_77t1:c.1767C>T | NP_000206.2:p.Gly589= | |
| XM_005259896.2:c.1896C>T | XP_005259953.1:p.Gly632= | |
| XM_006722745.2:c.1767C>T | XP_006722808.1:p.Gly589= | |
| XM_011527990.1:c.1896C>T | XP_011526292.1:p.Gly632= | |
| XM_011527991.1:c.1896C>T | XP_011526293.1:p.Gly632= | |
| XR_430137.2:n.1906C>T | ||
| XM_005259896.3:c.1896C>T | XP_005259953.1:p.Gly632= | |
| XM_011527991.2:c.1896C>T | XP_011526293.1:p.Gly632= | |
| NM_000215.4:c.1767C>T MANE Select | NP_000206.2:p.Gly589= |