Linked Data
MyVariant Identifiers:
chr9:g.139571422G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136676970G>C , CM000671.2:g.136676970G>C | GRCh38 |
| NC_000009.11:g.139571422G>C , CM000671.1:g.139571422G>C | GRCh37 |
| NC_000009.10:g.138691243G>C | NCBI36 |
| NG_008090.1:g.15490C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371696.7:c.483C>G MANE Select | ENSP00000360761.2:p.Val161= | |
| ENST00000371694.7:c.483C>G | ENSP00000360759.3:p.Val161= | |
| ENST00000371696.6:c.483C>G | ENSP00000360761.2:p.Val161= | |
| ENST00000472820.1:n.411C>G | ||
| ENST00000538402.1:c.483C>G | ENSP00000438919.1:p.Val161= | |
| NM_001012727.1:c.483C>G | NP_001012745.1:p.Val161= | |
| NM_006412.3:c.483C>G | NP_006403.2:p.Val161= | |
| NM_006412.4:c.483C>G MANE Select | NP_006403.2:p.Val161= | |
| NM_001012727.2:c.483C>G | NP_001012745.1:p.Val161= |