Linked Data
ClinVar Variation Id:
1139872
ClinVar RCV Id:
RCV001476713
dbSNP Id:
rs2132076997
gnomAD v4:
9-34506832-C-T
MyVariant Identifiers:
chr9:g.34506830C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.34506832C>T , CM000671.2:g.34506832C>T | GRCh38 |
| NC_000009.11:g.34506830C>T , CM000671.1:g.34506830C>T | GRCh37 |
| NC_000009.10:g.34496830C>T | NCBI36 |
| NG_008127.1:g.53020C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242317.9:c.1269C>T MANE Select | ENSP00000242317.4:p.Cys423= | |
| ENST00000242317.8:c.1269C>T | ENSP00000242317.4:p.Cys423= | |
| ENST00000470169.5:c.206C>T | ||
| ENST00000614641.4:c.1281C>T | ENSP00000480538.1:p.Cys427= | |
| NM_001281428.1:c.1281C>T | NP_001268357.1:p.Cys427= | |
| NM_012144.3:c.1269C>T | NP_036276.1:p.Cys423= | |
| XM_006716758.2:c.738C>T | XP_006716821.1:p.Cys246= | |
| XM_011517846.1:c.1281C>T | XP_011516148.1:p.Cys427= | |
| XM_011517847.1:c.1281C>T | XP_011516149.1:p.Cys427= | |
| XM_011517848.1:c.1281C>T | XP_011516150.1:p.Cys427= | |
| XM_011517849.1:c.1281C>T | XP_011516151.1:p.Cys427= | |
| XM_011517850.1:c.1281C>T | XP_011516152.1:p.Cys427= | |
| XR_929232.1:n.1535C>T | ||
| XR_929233.1:n.1535C>T | ||
| XR_929235.1:n.1535C>T | ||
| XM_006716758.3:c.738C>T | XP_006716821.1:p.Cys246= | |
| XM_011517846.2:c.1281C>T | XP_011516148.1:p.Cys427= | |
| XM_011517847.3:c.1281C>T | XP_011516149.1:p.Cys427= | |
| XM_011517848.2:c.1281C>T | XP_011516150.1:p.Cys427= | |
| XM_011517849.2:c.1281C>T | XP_011516151.1:p.Cys427= | |
| XM_011517850.3:c.1281C>T | XP_011516152.1:p.Cys427= | |
| XM_017014625.2:c.1269C>T | XP_016870114.1:p.Cys423= | |
| XR_002956774.1:n.1482C>T | ||
| XR_929232.2:n.1482C>T | ||
| XR_929233.2:n.1482C>T | ||
| NM_012144.4:c.1269C>T MANE Select | NP_036276.1:p.Cys423= | |
| NM_001281428.2:c.1281C>T | NP_001268357.1:p.Cys427= |