Canonical Allele Identifier: CA2193710138
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419292A= , CM000677.2:g.87419292A= GRCh38
NC_000015.9:g.87962523A= , CM000677.1:g.87962523A= GRCh37
NC_000015.8:g.85763527A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-21T=
XR_932585.1:n.340-21T=
XR_001751647.1:n.617-21T=
XR_932585.2:n.627-21T=