Canonical Allele Identifier: CA2566922713
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072551G>T , CM000673.2:g.116072551G>T GRCh38
NC_000011.9:g.115943269G>T , CM000673.1:g.115943269G>T GRCh37
NC_000011.8:g.115448479G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+463C>A
XR_948056.1:n.311-5346C>A
XR_948057.1:n.97+558C>A
XR_001748401.1:n.192+463C>A
XR_948055.2:n.192+463C>A
XR_948056.2:n.314-5346C>A
XR_948057.2:n.97+558C>A