Linked Data
MyVariant Identifiers:
chr12:g.21349923T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21196989T>A , CM000674.2:g.21196989T>A | GRCh38 |
| NC_000012.11:g.21349923T>A , CM000674.1:g.21349923T>A | GRCh37 |
| NC_000012.10:g.21241190T>A | NCBI36 |
| NG_011745.1:g.70796T>A , LRG_1022:g.70796T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.771T>A MANE Select | ENSP00000256958.2:p.Ala257= | |
| ENST00000256958.2:c.771T>A | ENSP00000256958.2:p.Ala257= | |
| NM_006446.4:c.771T>A , LRG_1022t1:c.771T>A | NP_006437.3:p.Ala257= | |
| NM_006446.5:c.771T>A MANE Select | NP_006437.3:p.Ala257= |