Canonical Allele Identifier: CA1106753688
Gene:

Linked Data

dbSNP Id: rs1795645915

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306307A>G , CM000669.2:g.124306307A>G GRCh38
NC_000007.13:g.123946361A>G , CM000669.1:g.123946361A>G GRCh37
NC_000007.12:g.123733597A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-171A>G