Canonical Allele Identifier: CA651610722
Gene:

Linked Data

dbSNP Id: rs1050845902

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400545G>T , CM000669.2:g.13400545G>T GRCh38
NC_000007.13:g.13440170G>T , CM000669.1:g.13440170G>T GRCh37
NC_000007.12:g.13406695G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90222G>T