Linked Data
MyVariant Identifiers:
chr12:g.58158286G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764503G>T , CM000674.2:g.57764503G>T | GRCh38 |
| NC_000012.11:g.58158286G>T , CM000674.1:g.58158286G>T | GRCh37 |
| NC_000012.10:g.56444553G>T | NCBI36 |
| NG_007076.1:g.7691C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1092C>A | ENSP00000518840.1:p.Pro364= | |
| ENST00000713545.1:c.*16C>A | ENSP00000518841.1:n.*16C>A | |
| ENST00000228606.9:c.1011C>A MANE Select | ENSP00000228606.4:p.Pro337= | |
| ENST00000228606.8:c.1011C>A | ENSP00000228606.4:p.Pro337= | |
| ENST00000546567.5:c.306C>A | ENSP00000449472.1:p.Pro102= | |
| ENST00000547344.5:n.1150C>A | ||
| NM_000785.3:c.1011C>A | NP_000776.1:p.Pro337= | |
| NM_000785.4:c.1011C>A MANE Select | NP_000776.1:p.Pro337= |