Canonical Allele Identifier: CA2193710691
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419500T= , CM000677.2:g.87419500T= GRCh38
NC_000015.9:g.87962731T= , CM000677.1:g.87962731T= GRCh37
NC_000015.8:g.85763735T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-229A=
XR_932585.1:n.340-229A=
XR_001751647.1:n.617-229A=
XR_932585.2:n.627-229A=