Canonical Allele Identifier: CA963163198
Gene:

Linked Data

dbSNP Id: rs2034712754

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417583A>T , CM000676.2:g.52417583A>T GRCh38
NC_000014.8:g.52884301A>T , CM000676.1:g.52884301A>T GRCh37
NC_000014.7:g.51954051A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3120T>A