Linked Data
MyVariant Identifiers:
chr12:g.58157435T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763652T>G , CM000674.2:g.57763652T>G | GRCh38 |
| NC_000012.11:g.58157435T>G , CM000674.1:g.58157435T>G | GRCh37 |
| NC_000012.10:g.56443702T>G | NCBI36 |
| NG_007076.1:g.8542A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1453A>C | ENSP00000518840.1:p.Arg485= | |
| ENST00000713545.1:c.*377A>C | ENSP00000518841.1:n.*377A>C | |
| ENST00000228606.9:c.1372A>C MANE Select | ENSP00000228606.4:p.Arg458= | |
| ENST00000228606.8:c.1372A>C | ENSP00000228606.4:p.Arg458= | |
| ENST00000547344.5:n.1511A>C | ||
| NM_000785.3:c.1372A>C | NP_000776.1:p.Arg458= | |
| NM_000785.4:c.1372A>C MANE Select | NP_000776.1:p.Arg458= |