Linked Data
MyVariant Identifiers:
chr12:g.58158891G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57765108G>C , CM000674.2:g.57765108G>C | GRCh38 |
| NC_000012.11:g.58158891G>C , CM000674.1:g.58158891G>C | GRCh37 |
| NC_000012.10:g.56445158G>C | NCBI36 |
| NG_007076.1:g.7086C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000546609.2:n.605C>G | ||
| ENST00000713544.1:c.774C>G | ENSP00000518840.1:p.Ser258= | |
| ENST00000713545.1:c.751C>G | ENSP00000518841.1:p.His251Asp | |
| ENST00000228606.9:c.693C>G MANE Select | ENSP00000228606.4:p.Ser231= | |
| ENST00000228606.8:c.693C>G | ENSP00000228606.4:p.Ser231= | |
| ENST00000546567.5:c.-13C>G | ENSP00000449472.1:n.-13C>G | |
| ENST00000546609.1:c.605C>G | ||
| ENST00000547344.5:n.832C>G | ||
| ENST00000547451.1:n.493C>G | ||
| NM_000785.3:c.693C>G | NP_000776.1:p.Ser231= | |
| NM_000785.4:c.693C>G MANE Select | NP_000776.1:p.Ser231= |