Linked Data
ClinVar Variation Id:
2849723
ClinVar RCV Id:
RCV003652626
dbSNP Id:
rs2132077032
COSMIC:
COSM5765348
MyVariant Identifiers:
chr9:g.34506866G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.34506868G>A , CM000671.2:g.34506868G>A | GRCh38 |
| NC_000009.11:g.34506866G>A , CM000671.1:g.34506866G>A | GRCh37 |
| NC_000009.10:g.34496866G>A | NCBI36 |
| NG_008127.1:g.53056G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242317.9:c.1305G>A MANE Select | ENSP00000242317.4:p.Val435= | |
| ENST00000242317.8:c.1305G>A | ENSP00000242317.4:p.Val435= | |
| ENST00000470169.5:c.242G>A | ||
| ENST00000614641.4:c.1317G>A | ENSP00000480538.1:p.Val439= | |
| NM_001281428.1:c.1317G>A | NP_001268357.1:p.Val439= | |
| NM_012144.3:c.1305G>A | NP_036276.1:p.Val435= | |
| XM_006716758.2:c.774G>A | XP_006716821.1:p.Val258= | |
| XM_011517846.1:c.1317G>A | XP_011516148.1:p.Val439= | |
| XM_011517847.1:c.1317G>A | XP_011516149.1:p.Val439= | |
| XM_011517848.1:c.1317G>A | XP_011516150.1:p.Val439= | |
| XM_011517849.1:c.1317G>A | XP_011516151.1:p.Val439= | |
| XM_011517850.1:c.1317G>A | XP_011516152.1:p.Val439= | |
| XR_929232.1:n.1571G>A | ||
| XR_929233.1:n.1571G>A | ||
| XR_929235.1:n.1571G>A | ||
| XM_006716758.3:c.774G>A | XP_006716821.1:p.Val258= | |
| XM_011517846.2:c.1317G>A | XP_011516148.1:p.Val439= | |
| XM_011517847.3:c.1317G>A | XP_011516149.1:p.Val439= | |
| XM_011517848.2:c.1317G>A | XP_011516150.1:p.Val439= | |
| XM_011517849.2:c.1317G>A | XP_011516151.1:p.Val439= | |
| XM_011517850.3:c.1317G>A | XP_011516152.1:p.Val439= | |
| XM_017014625.2:c.1305G>A | XP_016870114.1:p.Val435= | |
| XR_002956774.1:n.1518G>A | ||
| XR_929232.2:n.1518G>A | ||
| XR_929233.2:n.1518G>A | ||
| NM_012144.4:c.1305G>A MANE Select | NP_036276.1:p.Val435= | |
| NM_001281428.2:c.1317G>A | NP_001268357.1:p.Val439= |