Linked Data
dbSNP Id:
rs779574872
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5046034G>A , CM000674.2:g.5046034G>A | GRCh38 |
| NC_000012.11:g.5155200G>A , CM000674.1:g.5155200G>A | GRCh37 |
| NC_000012.10:g.5025461G>A | NCBI36 |
| NG_012198.1:g.7116G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.*45G>A MANE Select | ENSP00000252321.3:n.*45G>A | |
| ENST00000252321.4:c.*45G>A | ENSP00000252321.3:n.*45G>A | |
| NM_002234.3:c.*45G>A | NP_002225.2:n.*45G>A | |
| NM_002234.4:c.*45G>A MANE Select | NP_002225.2:n.*45G>A |