Canonical Allele Identifier: CA2761911337
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558398A>G , CM000666.2:g.62558398A>G GRCh38
NC_000004.11:g.63424116A>G , CM000666.1:g.63424116A>G GRCh37
NC_000004.10:g.63106711A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5446A>G