Canonical Allele Identifier: CA2267413191
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788867A= , CM000679.2:g.57788867A= GRCh38
NC_000017.10:g.55866228A= , CM000679.1:g.55866228A= GRCh37
NC_000017.9:g.53221227A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16671T=
XR_934881.3:n.3815-16671T=