Canonical Allele Identifier: CA2705985308
Gene:

Linked Data

dbSNP Id: rs2109569182

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557907A>C , CM000666.2:g.62557907A>C GRCh38
NC_000004.11:g.63423625A>C , CM000666.1:g.63423625A>C GRCh37
NC_000004.10:g.63106220A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5937A>C