Canonical Allele Identifier: CA652528299
Gene:

Linked Data

dbSNP Id: rs1810441785

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535715G>A , CM000670.2:g.88535715G>A GRCh38
NC_000008.10:g.89547944G>A , CM000670.1:g.89547944G>A GRCh37
NC_000008.9:g.89617060G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10802C>T
XR_001745653.2:n.286-6965G>A
XR_928383.3:n.1475+10802C>T