Linked Data
dbSNP Id:
rs1713606653
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24795004C>A , CM000666.2:g.24795004C>A | GRCh38 |
| NC_000004.11:g.24796626C>A , CM000666.1:g.24796626C>A | GRCh37 |
| NC_000004.10:g.24405724C>A | NCBI36 |
| NG_012213.1:g.4542C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-16-4502C>A | ENSP00000472134.1:n.-16-4502C>A |