Canonical Allele Identifier:
CA1282456406
Gene:
Linked Data
dbSNP Id:
rs1678006168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.118079570G>T , CM000664.2:g.118079570G>T | GRCh38 |
| NC_000002.11:g.118837146G>T , CM000664.1:g.118837146G>T | GRCh37 |
| NC_000002.10:g.118553616G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512305.1:c.697-2038C>A | XP_011510607.1:n.697-2038C>A | |
| XR_001739662.2:n.138+8681C>A |