Canonical Allele Identifier: CA1250829385
Gene:

Linked Data

dbSNP Id: rs1284714089

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722436T>G , CM000664.2:g.52722436T>G GRCh38
NC_000002.11:g.52949574T>G , CM000664.1:g.52949574T>G GRCh37
NC_000002.10:g.52803078T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.821A>C