Canonical Allele Identifier: CA691969184
Gene:

Linked Data

dbSNP Id: rs1268519190

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004986G>A , CM000674.2:g.76004986G>A GRCh38
NC_000012.11:g.76398766G>A , CM000674.1:g.76398766G>A GRCh37
NC_000012.10:g.74685033G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1203C>T
XR_001749218.2:n.402+1203C>T
XR_945110.3:n.402+1203C>T