Canonical Allele Identifier: CA1218511533
Gene:

Linked Data

dbSNP Id: rs1045614747

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198500044G>A , CM000663.2:g.198500044G>A GRCh38
NC_000001.10:g.198469174G>A , CM000663.1:g.198469174G>A GRCh37
NC_000001.9:g.196735797G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922398.1:n.679+19507C>T
XR_922398.2:n.341+19507C>T