Canonical Allele Identifier: CA1250829442
Gene:

Linked Data

dbSNP Id: rs1668663059

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722528T>C , CM000664.2:g.52722528T>C GRCh38
NC_000002.11:g.52949666T>C , CM000664.1:g.52949666T>C GRCh37
NC_000002.10:g.52803170T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.729A>G