Canonical Allele Identifier: CA1740470102
Gene:

Linked Data

dbSNP Id: rs1795645873

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306304A>G , CM000669.2:g.124306304A>G GRCh38
NC_000007.13:g.123946358A>G , CM000669.1:g.123946358A>G GRCh37
NC_000007.12:g.123733594A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-174A>G