Canonical Allele Identifier: CA963163229
Gene:

Linked Data

dbSNP Id: rs2034713524

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417640A>G , CM000676.2:g.52417640A>G GRCh38
NC_000014.8:g.52884358A>G , CM000676.1:g.52884358A>G GRCh37
NC_000014.7:g.51954108A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3063T>C