Canonical Allele Identifier: CA2293960138
Gene:

Linked Data

dbSNP Id: rs2031432744

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756638G>A , CM000680.2:g.31756638G>A GRCh38
NC_000018.9:g.29336601G>A , CM000680.1:g.29336601G>A GRCh37
NC_000018.8:g.27590599G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5501G>A