Linked Data
MyVariant Identifiers:
chr3:g.186257282C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186539493C>A , CM000665.2:g.186539493C>A | GRCh38 |
| NC_000003.11:g.186257282C>A , CM000665.1:g.186257282C>A | GRCh37 |
| NC_000003.10:g.187739976C>A | NCBI36 |
| NG_009829.1:g.9886G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307944.6:c.126G>T MANE Select | ENSP00000312099.5:p.Val42= | |
| ENST00000307944.5:c.126G>T | ENSP00000312099.5:p.Val42= | |
| ENST00000392499.6:c.126G>T | ENSP00000376287.2:p.Val42= | |
| ENST00000460288.1:n.1028G>T | ||
| NM_017541.2:c.126G>T | NP_060011.1:p.Val42= | |
| NM_017541.3:c.126G>T | NP_060011.1:p.Val42= | |
| NM_017541.4:c.126G>T MANE Select | NP_060011.1:p.Val42= |