Canonical Allele Identifier: CA1106753665
Gene:

Linked Data

dbSNP Id: rs1795645636

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306270A>G , CM000669.2:g.124306270A>G GRCh38
NC_000007.13:g.123946324A>G , CM000669.1:g.123946324A>G GRCh37
NC_000007.12:g.123733560A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-208A>G