Canonical Allele Identifier: CA220638147
Gene:

Linked Data

dbSNP Id: rs113616880

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759292C>A , CM000673.2:g.34759292C>A GRCh38
NC_000011.9:g.34780839C>A , CM000673.1:g.34780839C>A GRCh37
NC_000011.8:g.34737415C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+4685C>A
XR_931188.1:n.693+4685C>A
XR_931189.1:n.854+4685C>A
XR_931190.1:n.639+4685C>A
XR_931191.1:n.689+4685C>A
XR_001748174.1:n.855+4685C>A
XR_001748176.1:n.1016+4685C>A
XR_002957246.1:n.639+4685C>A