Canonical Allele Identifier: CA2193585422
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152190C= , CM000677.2:g.87152190C= GRCh38
NC_000015.9:g.87695421C= , CM000677.1:g.87695421C= GRCh37
NC_000015.8:g.85496425C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26037C=
XR_932582.2:n.167-26037C=