Canonical Allele Identifier: CA1063282173
Gene:

Linked Data

dbSNP Id: rs763114425

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558223T>A , CM000666.2:g.62558223T>A GRCh38
NC_000004.11:g.63423941T>A , CM000666.1:g.63423941T>A GRCh37
NC_000004.10:g.63106536T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5621T>A