Linked Data
dbSNP Id:
rs2084770830
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530525A>C , CM000665.2:g.129530525A>C | GRCh38 |
| NC_000003.11:g.129249368A>C , CM000665.1:g.129249368A>C | GRCh37 |
| NC_000003.10:g.130732058A>C | NCBI36 |
| NG_009115.1:g.6887A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.362-351A>C MANE Select | ENSP00000296271.3:n.362-351A>C | |
| ENST00000296271.3:c.362-351A>C | ENSP00000296271.3:n.362-351A>C | |
| NM_000539.3:c.362-351A>C MANE Select | NP_000530.1:n.362-351A>C |