Canonical Allele Identifier: CA2724463165
Gene:

Linked Data

dbSNP Id: rs2134908317

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851732A>T , CM000673.2:g.80851732A>T GRCh38
NC_000011.9:g.80562775A>T , CM000673.1:g.80562775A>T GRCh37
NC_000011.8:g.80240423A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60559T>A