Linked Data
MyVariant Identifiers:
chr12:g.91449297G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91055520G>T , CM000674.2:g.91055520G>T | GRCh38 |
| NC_000012.11:g.91449297G>T , CM000674.1:g.91449297G>T | GRCh37 |
| NC_000012.10:g.89973428G>T | NCBI36 |
| NG_021223.1:g.7835C>A , LRG_538:g.7835C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266719.4:c.762C>A MANE Select | ENSP00000266719.3:p.Leu254= | |
| ENST00000266719.3:c.762C>A | ENSP00000266719.3:p.Leu254= | |
| NM_007035.3:c.762C>A , LRG_538t1:c.762C>A | NP_008966.1:p.Leu254= | |
| XM_011537781.1:c.762C>A | XP_011536083.1:p.Leu254= | |
| NM_007035.4:c.762C>A MANE Select | NP_008966.1:p.Leu254= |