Canonical Allele Identifier: CA778454215
Gene:

Linked Data

dbSNP Id: rs1211510491

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756668C>G , CM000680.2:g.31756668C>G GRCh38
NC_000018.9:g.29336631C>G , CM000680.1:g.29336631C>G GRCh37
NC_000018.8:g.27590629C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5471C>G