Canonical Allele Identifier: CA680793843
Gene:

Linked Data

dbSNP Id: rs1343701837

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.81143416A>C , CM000673.2:g.81143416A>C GRCh38
NC_000011.9:g.80854459A>C , CM000673.1:g.80854459A>C GRCh37
NC_000011.8:g.80532107A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.46+109510T>G