Canonical Allele Identifier: CA2137107155
Gene:

Linked Data

dbSNP Id: rs2034713889

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417678G>A , CM000676.2:g.52417678G>A GRCh38
NC_000014.8:g.52884396G>A , CM000676.1:g.52884396G>A GRCh37
NC_000014.7:g.51954146G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3025C>T