Canonical Allele Identifier: CA2705985316
Gene:

Linked Data

dbSNP Id: rs2109569226

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558006T>C , CM000666.2:g.62558006T>C GRCh38
NC_000004.11:g.63423724T>C , CM000666.1:g.63423724T>C GRCh37
NC_000004.10:g.63106319T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5838T>C