Canonical Allele Identifier: CA1462694221
Gene:

Linked Data

dbSNP Id: rs1756227170

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558113C>G , CM000666.2:g.62558113C>G GRCh38
NC_000004.11:g.63423831C>G , CM000666.1:g.63423831C>G GRCh37
NC_000004.10:g.63106426C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5731C>G