Linked Data
MyVariant Identifiers:
chr12:g.91449219G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91055442G>A , CM000674.2:g.91055442G>A | GRCh38 |
| NC_000012.11:g.91449219G>A , CM000674.1:g.91449219G>A | GRCh37 |
| NC_000012.10:g.89973350G>A | NCBI36 |
| NG_021223.1:g.7913C>T , LRG_538:g.7913C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266719.4:c.840C>T MANE Select | ENSP00000266719.3:p.Ile280= | |
| ENST00000266719.3:c.840C>T | ENSP00000266719.3:p.Ile280= | |
| NM_007035.3:c.840C>T , LRG_538t1:c.840C>T | NP_008966.1:p.Ile280= | |
| XM_011537781.1:c.840C>T | XP_011536083.1:p.Ile280= | |
| NM_007035.4:c.840C>T MANE Select | NP_008966.1:p.Ile280= |