Canonical Allele Identifier: CA2193710695
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419501C= , CM000677.2:g.87419501C= GRCh38
NC_000015.9:g.87962732C= , CM000677.1:g.87962732C= GRCh37
NC_000015.8:g.85763736C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.339+228G=
XR_932585.1:n.339+228G=
XR_001751647.1:n.616+228G=
XR_932585.2:n.626+228G=