Canonical Allele Identifier: CA2189495318
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78406417C= , CM000677.2:g.78406417C= GRCh38
NC_000015.9:g.78698759C= , CM000677.1:g.78698759C= GRCh37
NC_000015.8:g.76485814C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932504.1:n.237-128C=
XR_932505.1:n.237-128C=
XR_932506.1:n.165C=
XR_932507.1:n.165C=
XR_932506.2:n.344C=