Canonical Allele Identifier: CA2193710351
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419363C= , CM000677.2:g.87419363C= GRCh38
NC_000015.9:g.87962594C= , CM000677.1:g.87962594C= GRCh37
NC_000015.8:g.85763598C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-92G=
XR_932585.1:n.340-92G=
XR_001751647.1:n.617-92G=
XR_932585.2:n.627-92G=