Linked Data
dbSNP Id:
rs1560188338
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24794870A>G , CM000666.2:g.24794870A>G | GRCh38 |
| NC_000004.11:g.24796492A>G , CM000666.1:g.24796492A>G | GRCh37 |
| NC_000004.10:g.24405590A>G | NCBI36 |
| NG_012213.1:g.4408A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-16-4636A>G | ENSP00000472134.1:n.-16-4636A>G |