Linked Data
MyVariant Identifiers:
chr12:g.58157950A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764167A>T , CM000674.2:g.57764167A>T | GRCh38 |
| NC_000012.11:g.58157950A>T , CM000674.1:g.58157950A>T | GRCh37 |
| NC_000012.10:g.56444217A>T | NCBI36 |
| NG_007076.1:g.8027T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1227T>A | ENSP00000518840.1:p.Pro409= | |
| ENST00000713545.1:c.*151T>A | ENSP00000518841.1:n.*151T>A | |
| ENST00000228606.9:c.1146T>A MANE Select | ENSP00000228606.4:p.Pro382= | |
| ENST00000228606.8:c.1146T>A | ENSP00000228606.4:p.Pro382= | |
| ENST00000546567.5:c.441T>A | ENSP00000449472.1:p.Pro147= | |
| ENST00000547344.5:n.1285T>A | ||
| NM_000785.3:c.1146T>A | NP_000776.1:p.Pro382= | |
| NM_000785.4:c.1146T>A MANE Select | NP_000776.1:p.Pro382= |