Linked Data
MyVariant Identifiers:
chr3:g.81754656A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705505A>T , CM000665.2:g.81705505A>T | GRCh38 |
| NC_000003.11:g.81754656A>T , CM000665.1:g.81754656A>T | GRCh37 |
| NC_000003.10:g.81837346A>T | NCBI36 |
| NG_011810.1:g.61296T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.252T>A MANE Select | ENSP00000410833.2:p.Gly84= | |
| ENST00000429644.6:c.252T>A | ENSP00000410833.2:p.Gly84= | |
| ENST00000489715.1:c.129T>A | ENSP00000419638.1:p.Gly43= | |
| NM_000158.3:c.252T>A | NP_000149.3:p.Gly84= | |
| NM_000158.4:c.252T>A MANE Select | NP_000149.4:p.Gly84= |