Canonical Allele Identifier: CA936775892
Gene:

Linked Data

dbSNP Id: rs1851777170

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812662C>T , CM000673.2:g.34812662C>T GRCh38
NC_000011.9:g.34834209C>T , CM000673.1:g.34834209C>T GRCh37
NC_000011.8:g.34790785C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58055C>T
XR_931188.1:n.693+58055C>T
XR_931189.1:n.854+58055C>T
XR_931190.1:n.639+58055C>T
XR_931191.1:n.689+58055C>T
XR_001748174.1:n.855+58055C>T
XR_001748176.1:n.1016+58055C>T
XR_002957246.1:n.639+58055C>T