Canonical Allele Identifier: CA1963413281
Gene:

Linked Data

dbSNP Id: rs1851773898

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812428G>A , CM000673.2:g.34812428G>A GRCh38
NC_000011.9:g.34833975G>A , CM000673.1:g.34833975G>A GRCh37
NC_000011.8:g.34790551G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57821G>A
XR_931188.1:n.693+57821G>A
XR_931189.1:n.854+57821G>A
XR_931190.1:n.639+57821G>A
XR_931191.1:n.689+57821G>A
XR_001748174.1:n.855+57821G>A
XR_001748176.1:n.1016+57821G>A
XR_002957246.1:n.639+57821G>A