Linked Data
MyVariant Identifiers:
chr3:g.122060289C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122341442C>A , CM000665.2:g.122341442C>A | GRCh38 |
| NC_000003.11:g.122060289C>A , CM000665.1:g.122060289C>A | GRCh37 |
| NC_000003.10:g.123542979C>A | NCBI36 |
| NG_027995.1:g.21279C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264474.4:c.172C>A MANE Select | ENSP00000264474.3:p.Arg58= | |
| ENST00000264474.3:c.172C>A | ENSP00000264474.3:p.Arg58= | |
| NM_005213.3:c.172C>A | NP_005204.1:p.Arg58= | |
| NM_005213.4:c.172C>A MANE Select | NP_005204.1:p.Arg58= |