Linked Data
MyVariant Identifiers:
chr12:g.91449270T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91055493T>A , CM000674.2:g.91055493T>A | GRCh38 |
| NC_000012.11:g.91449270T>A , CM000674.1:g.91449270T>A | GRCh37 |
| NC_000012.10:g.89973401T>A | NCBI36 |
| NG_021223.1:g.7862A>T , LRG_538:g.7862A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266719.4:c.789A>T MANE Select | ENSP00000266719.3:p.Ser263= | |
| ENST00000266719.3:c.789A>T | ENSP00000266719.3:p.Ser263= | |
| NM_007035.3:c.789A>T , LRG_538t1:c.789A>T | NP_008966.1:p.Ser263= | |
| XM_011537781.1:c.789A>T | XP_011536083.1:p.Ser263= | |
| NM_007035.4:c.789A>T MANE Select | NP_008966.1:p.Ser263= |