Canonical Allele Identifier: CA220644008
Gene:

Linked Data

dbSNP Id: rs12791769

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812721A>G , CM000673.2:g.34812721A>G GRCh38
NC_000011.9:g.34834268A>G , CM000673.1:g.34834268A>G GRCh37
NC_000011.8:g.34790844A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58114A>G
XR_931188.1:n.693+58114A>G
XR_931189.1:n.854+58114A>G
XR_931190.1:n.639+58114A>G
XR_931191.1:n.689+58114A>G
XR_001748174.1:n.855+58114A>G
XR_001748176.1:n.1016+58114A>G
XR_002957246.1:n.639+58114A>G