Canonical Allele Identifier: CA1985859967
Gene:

Linked Data

dbSNP Id: rs1271835037

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851729C>T , CM000673.2:g.80851729C>T GRCh38
NC_000011.9:g.80562772C>T , CM000673.1:g.80562772C>T GRCh37
NC_000011.8:g.80240420C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60562G>A