Canonical Allele Identifier: CA2705985313
Gene:

Linked Data

dbSNP Id: rs2109569196

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557945A>G , CM000666.2:g.62557945A>G GRCh38
NC_000004.11:g.63423663A>G , CM000666.1:g.63423663A>G GRCh37
NC_000004.10:g.63106258A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5899A>G