Linked Data
ClinVar Variation Id:
3224732
ClinVar RCV Id:
RCV004521422
gnomAD v4:
9-104828922-G-T
MyVariant Identifiers:
chr9:g.107591203G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.104828922G>T , CM000671.2:g.104828922G>T | GRCh38 |
| NC_000009.11:g.107591203G>T , CM000671.1:g.107591203G>T | GRCh37 |
| NC_000009.10:g.106631024G>T | NCBI36 |
| NG_007981.1:g.104234C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374736.8:c.2109C>A MANE Select | ENSP00000363868.3:p.Ile703= | |
| ENST00000678995.1:c.2109C>A | ENSP00000504612.1:p.Ile703= | |
| ENST00000374736.7:c.2109C>A | ENSP00000363868.3:p.Ile703= | |
| ENST00000494467.1:n.282C>A | ||
| NM_005502.3:c.2109C>A | NP_005493.2:p.Ile703= | |
| XM_005251773.1:c.2109C>A | XP_005251830.1:p.Ile703= | |
| XM_005251776.1:c.1929C>A | XP_005251833.1:p.Ile643= | |
| XM_011518339.1:c.2184C>A | XP_011516641.1:p.Ile728= | |
| XM_011518340.1:c.2184C>A | XP_011516642.1:p.Ile728= | |
| XM_011518341.1:c.2184C>A | XP_011516643.1:p.Ile728= | |
| XM_011518342.1:c.1746C>A | XP_011516644.1:p.Ile582= | |
| XM_011518343.1:c.2184C>A | XP_011516645.1:p.Ile728= | |
| XM_011518344.1:c.2184C>A | XP_011516646.1:p.Ile728= | |
| XM_005251773.3:c.2109C>A | XP_005251830.1:p.Ile703= | |
| XM_005251776.3:c.1929C>A | XP_005251833.1:p.Ile643= | |
| XM_011518339.3:c.2184C>A | XP_011516641.1:p.Ile728= | |
| XM_011518340.3:c.2184C>A | XP_011516642.1:p.Ile728= | |
| XM_011518341.3:c.2184C>A | XP_011516643.1:p.Ile728= | |
| XM_011518342.3:c.1746C>A | XP_011516644.1:p.Ile582= | |
| XM_011518344.2:c.2184C>A | XP_011516646.1:p.Ile728= | |
| XM_017014378.2:c.2184C>A | XP_016869867.1:p.Ile728= | |
| XM_017014379.2:c.2184C>A | XP_016869868.1:p.Ile728= | |
| XM_017014380.2:c.2184C>A | XP_016869869.1:p.Ile728= | |
| XM_017014381.2:c.2184C>A | XP_016869870.1:p.Ile728= | |
| XM_017014382.2:c.2046C>A | XP_016869871.1:p.Ile682= | |
| XR_001746223.1:n.2497C>A | ||
| NM_005502.4:c.2109C>A MANE Select | NP_005493.2:p.Ile703= |