Canonical Allele Identifier: CA220644004
Gene:

Linked Data

dbSNP Id: rs997009505

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812699C>A , CM000673.2:g.34812699C>A GRCh38
NC_000011.9:g.34834246C>A , CM000673.1:g.34834246C>A GRCh37
NC_000011.8:g.34790822C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58092C>A
XR_931188.1:n.693+58092C>A
XR_931189.1:n.854+58092C>A
XR_931190.1:n.639+58092C>A
XR_931191.1:n.689+58092C>A
XR_001748174.1:n.855+58092C>A
XR_001748176.1:n.1016+58092C>A
XR_002957246.1:n.639+58092C>A