Canonical Allele Identifier: CA1691656500
Gene:

Linked Data

dbSNP Id: rs1803287377

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957959A>G , CM000669.2:g.17957959A>G GRCh38
NC_000007.13:g.17997582A>G , CM000669.1:g.17997582A>G GRCh37
NC_000007.12:g.17964107A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-711A>G