Canonical Allele Identifier: CA1800733853
Gene:

Linked Data

dbSNP Id: rs1810441824

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535717C>A , CM000670.2:g.88535717C>A GRCh38
NC_000008.10:g.89547946C>A , CM000670.1:g.89547946C>A GRCh37
NC_000008.9:g.89617062C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10800G>T
XR_001745653.2:n.286-6963C>A
XR_928383.3:n.1475+10800G>T