Linked Data
MyVariant Identifiers:
chr9:g.139571103A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136676651A>C , CM000671.2:g.136676651A>C | GRCh38 |
| NC_000009.11:g.139571103A>C , CM000671.1:g.139571103A>C | GRCh37 |
| NC_000009.10:g.138690924A>C | NCBI36 |
| NG_008090.1:g.15809T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.522T>G MANE Select | ENSP00000360761.2:p.Thr174= | |
| ENST00000371694.7:c.492+310T>G | ENSP00000360759.3:n.492+310T>G | |
| ENST00000371696.6:c.522T>G | ENSP00000360761.2:p.Thr174= | |
| ENST00000472820.1:n.450T>G | ||
| ENST00000538402.1:c.522T>G | ENSP00000438919.1:p.Thr174= | |
| NM_001012727.1:c.492+310T>G | NP_001012745.1:n.492+310T>G | |
| NM_006412.3:c.522T>G | NP_006403.2:p.Thr174= | |
| NM_006412.4:c.522T>G MANE Select | NP_006403.2:p.Thr174= | |
| NM_001012727.2:c.492+310T>G | NP_001012745.1:n.492+310T>G |