Canonical Allele Identifier: CA1963413405
Gene:

Linked Data

dbSNP Id: rs1851777220

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812664T>G , CM000673.2:g.34812664T>G GRCh38
NC_000011.9:g.34834211T>G , CM000673.1:g.34834211T>G GRCh37
NC_000011.8:g.34790787T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58057T>G
XR_931188.1:n.693+58057T>G
XR_931189.1:n.854+58057T>G
XR_931190.1:n.639+58057T>G
XR_931191.1:n.689+58057T>G
XR_001748174.1:n.855+58057T>G
XR_001748176.1:n.1016+58057T>G
XR_002957246.1:n.639+58057T>G