Canonical Allele Identifier: CA1932346132
Gene:

Linked Data

dbSNP Id: rs2064898794

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750650T>A , CM000672.2:g.101750650T>A GRCh38
NC_000010.10:g.103510407T>A , CM000672.1:g.103510407T>A GRCh37
NC_000010.9:g.103500397T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6433A>T
XR_946255.2:n.217-6433A>T