Canonical Allele Identifier: CA2193710577
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419470T= , CM000677.2:g.87419470T= GRCh38
NC_000015.9:g.87962701T= , CM000677.1:g.87962701T= GRCh37
NC_000015.8:g.85763705T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-199A=
XR_932585.1:n.340-199A=
XR_001751647.1:n.617-199A=
XR_932585.2:n.627-199A=