Linked Data
MyVariant Identifiers:
chr3:g.183777776C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184059988C>A , CM000665.2:g.184059988C>A | GRCh38 |
| NC_000003.11:g.183777776C>A , CM000665.1:g.183777776C>A | GRCh37 |
| NC_000003.10:g.185260470C>A | NCBI36 |
| NG_012749.1:g.11942C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1086C>A MANE Select | ENSP00000322617.1:p.Pro362= | |
| ENST00000318351.1:c.1086C>A | ENSP00000322617.1:p.Pro362= | |
| NM_130770.2:c.1086C>A | NP_570126.2:p.Pro362= | |
| NM_130770.3:c.1086C>A MANE Select | NP_570126.2:p.Pro362= |