Linked Data
dbSNP Id:
rs770996893
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.116461765C>A , CM000665.2:g.116461765C>A | GRCh38 |
| NC_000003.11:g.116180612C>A , CM000665.1:g.116180612C>A | GRCh37 |
| NC_000003.10:g.117663302C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474851.1:c.179-16810G>T | ENSP00000418506.1:n.179-16810G>T |