Canonical Allele Identifier: CA2716661689
Gene:

Linked Data

dbSNP Id: rs996659087

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735051G>T , CM000670.2:g.20735051G>T GRCh38
NC_000008.10:g.20592562G>T , CM000670.1:g.20592562G>T GRCh37
NC_000008.9:g.20636842G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55395G>T