Canonical Allele Identifier: CA2705977141
Gene:

Linked Data

dbSNP Id: rs2109569345

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558205A>G , CM000666.2:g.62558205A>G GRCh38
NC_000004.11:g.63423923A>G , CM000666.1:g.63423923A>G GRCh37
NC_000004.10:g.63106518A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5639A>G