Canonical Allele Identifier: CA220644001
Gene:

Linked Data

dbSNP Id: rs567825234

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812673A>G , CM000673.2:g.34812673A>G GRCh38
NC_000011.9:g.34834220A>G , CM000673.1:g.34834220A>G GRCh37
NC_000011.8:g.34790796A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58066A>G
XR_931188.1:n.693+58066A>G
XR_931189.1:n.854+58066A>G
XR_931190.1:n.639+58066A>G
XR_931191.1:n.689+58066A>G
XR_001748174.1:n.855+58066A>G
XR_001748176.1:n.1016+58066A>G
XR_002957246.1:n.639+58066A>G