Linked Data
dbSNP Id:
rs2037067932
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.111333861G>A , CM000665.2:g.111333861G>A | GRCh38 |
| NC_000003.11:g.111052708G>A , CM000665.1:g.111052708G>A | GRCh37 |
| NC_000003.10:g.112535398G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460744.1:c.-325-30652G>A | ENSP00000475194.1:n.-325-30652G>A | |
| XR_924332.1:n.163+27343G>A |