Linked Data
dbSNP Id:
rs2059017434
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240875189A>C , CM000664.2:g.240875189A>C | GRCh38 |
| NC_000002.11:g.241814606A>C , CM000664.1:g.241814606A>C | GRCh37 |
| NC_000002.10:g.241463279A>C | NCBI36 |
| NG_008005.1:g.11445A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.761A>C MANE Select | ENSP00000302620.3:p.Asp254Ala | |
| ENST00000307503.3:c.761A>C | ENSP00000302620.3:p.Asp254Ala | |
| ENST00000476698.1:n.413A>C | ||
| NM_000030.2:c.761A>C | NP_000021.1:p.Asp254Ala | |
| NM_000030.3:c.761A>C MANE Select | NP_000021.1:p.Asp254Ala |