Canonical Allele Identifier: CA220643960
Gene:

Linked Data

dbSNP Id: rs545509910

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812235G>T , CM000673.2:g.34812235G>T GRCh38
NC_000011.9:g.34833782G>T , CM000673.1:g.34833782G>T GRCh37
NC_000011.8:g.34790358G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57628G>T
XR_931188.1:n.693+57628G>T
XR_931189.1:n.854+57628G>T
XR_931190.1:n.639+57628G>T
XR_931191.1:n.689+57628G>T
XR_001748174.1:n.855+57628G>T
XR_001748176.1:n.1016+57628G>T
XR_002957246.1:n.639+57628G>T