Linked Data
ClinVar Variation Id:
1744871
ClinVar RCV Id:
RCV002335600
gnomAD v4:
9-104798514-C-T
MyVariant Identifiers:
chr9:g.107560795C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.104798514C>T , CM000671.2:g.104798514C>T | GRCh38 |
| NC_000009.11:g.107560795C>T , CM000671.1:g.107560795C>T | GRCh37 |
| NC_000009.10:g.106600616C>T | NCBI36 |
| NG_007981.1:g.134642G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374736.8:c.5028G>A MANE Select | ENSP00000363868.3:p.Leu1676= | |
| ENST00000678995.1:c.5034G>A | ENSP00000504612.1:p.Leu1678= | |
| ENST00000374736.7:c.5028G>A | ENSP00000363868.3:p.Leu1676= | |
| NM_005502.3:c.5028G>A | NP_005493.2:p.Leu1676= | |
| XM_005251773.1:c.5034G>A | XP_005251830.1:p.Leu1678= | |
| XM_005251776.1:c.4854G>A | XP_005251833.1:p.Leu1618= | |
| XM_011518339.1:c.5109G>A | XP_011516641.1:p.Leu1703= | |
| XM_011518340.1:c.5109G>A | XP_011516642.1:p.Leu1703= | |
| XM_011518341.1:c.5103G>A | XP_011516643.1:p.Leu1701= | |
| XM_011518342.1:c.4671G>A | XP_011516644.1:p.Leu1557= | |
| XM_011518343.1:c.5109G>A | XP_011516645.1:p.Leu1703= | |
| XM_005251773.3:c.5034G>A | XP_005251830.1:p.Leu1678= | |
| XM_005251776.3:c.4854G>A | XP_005251833.1:p.Leu1618= | |
| XM_011518339.3:c.5109G>A | XP_011516641.1:p.Leu1703= | |
| XM_011518340.3:c.5109G>A | XP_011516642.1:p.Leu1703= | |
| XM_011518341.3:c.5103G>A | XP_011516643.1:p.Leu1701= | |
| XM_011518342.3:c.4671G>A | XP_011516644.1:p.Leu1557= | |
| XM_017014378.2:c.5109G>A | XP_016869867.1:p.Leu1703= | |
| XM_017014379.2:c.5109G>A | XP_016869868.1:p.Leu1703= | |
| XM_017014380.2:c.5109G>A | XP_016869869.1:p.Leu1703= | |
| XM_017014381.2:c.5109G>A | XP_016869870.1:p.Leu1703= | |
| XM_017014382.2:c.4971G>A | XP_016869871.1:p.Leu1657= | |
| XR_001746223.1:n.5422G>A | ||
| NM_005502.4:c.5028G>A MANE Select | NP_005493.2:p.Leu1676= |