Linked Data
MyVariant Identifiers:
chr12:g.21329713C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21176779C>T , CM000674.2:g.21176779C>T | GRCh38 |
| NC_000012.11:g.21329713C>T , CM000674.1:g.21329713C>T | GRCh37 |
| NC_000012.10:g.21220980C>T | NCBI36 |
| NG_011745.1:g.50586C>T , LRG_1022:g.50586C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256958.3:c.363C>T MANE Select | ENSP00000256958.2:p.Tyr121= | |
| ENST00000256958.2:c.363C>T | ENSP00000256958.2:p.Tyr121= | |
| ENST00000543498.5:c.429C>T | ||
| NM_006446.4:c.363C>T , LRG_1022t1:c.363C>T | NP_006437.3:p.Tyr121= | |
| NM_006446.5:c.363C>T MANE Select | NP_006437.3:p.Tyr121= |