Linked Data
MyVariant Identifiers:
chr12:g.21331529G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21178595G>T , CM000674.2:g.21178595G>T | GRCh38 |
| NC_000012.11:g.21331529G>T , CM000674.1:g.21331529G>T | GRCh37 |
| NC_000012.10:g.21222796G>T | NCBI36 |
| NG_011745.1:g.52402G>T , LRG_1022:g.52402G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.501G>T MANE Select | ENSP00000256958.2:p.Gly167= | |
| ENST00000256958.2:c.501G>T | ENSP00000256958.2:p.Gly167= | |
| NM_006446.4:c.501G>T , LRG_1022t1:c.501G>T | NP_006437.3:p.Gly167= | |
| NM_006446.5:c.501G>T MANE Select | NP_006437.3:p.Gly167= |