Canonical Allele Identifier: CA988943689
Gene:

Linked Data

dbSNP Id: rs2031432086

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756602A>G , CM000680.2:g.31756602A>G GRCh38
NC_000018.9:g.29336565A>G , CM000680.1:g.29336565A>G GRCh37
NC_000018.8:g.27590563A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5537A>G