Canonical Allele Identifier: CA1462694114
Gene:

Linked Data

dbSNP Id: rs1756224656

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557917T>C , CM000666.2:g.62557917T>C GRCh38
NC_000004.11:g.63423635T>C , CM000666.1:g.63423635T>C GRCh37
NC_000004.10:g.63106230T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5927T>C