Linked Data
dbSNP Id:
rs1214019295
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442555G>T , CM000666.2:g.177442555G>T | GRCh38 |
| NC_000004.11:g.178363709G>T , CM000666.1:g.178363709G>T | GRCh37 |
| NC_000004.10:g.178600703G>T | NCBI36 |
| NG_011845.2:g.4949C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741929.1:n.56G>T |