Canonical Allele Identifier: CA2547802586
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072496C>A , CM000673.2:g.116072496C>A GRCh38
NC_000011.9:g.115943214C>A , CM000673.1:g.115943214C>A GRCh37
NC_000011.8:g.115448424C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+518G>T
XR_948056.1:n.311-5291G>T
XR_948057.1:n.97+613G>T
XR_001748401.1:n.192+518G>T
XR_948055.2:n.192+518G>T
XR_948056.2:n.314-5291G>T
XR_948057.2:n.97+613G>T