Canonical Allele Identifier: CA680801441
Gene:

Linked Data

dbSNP Id: rs1262412584

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851708A>C , CM000673.2:g.80851708A>C GRCh38
NC_000011.9:g.80562751A>C , CM000673.1:g.80562751A>C GRCh37
NC_000011.8:g.80240399A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60583T>G