Canonical Allele Identifier: CA2267413197
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788885C= , CM000679.2:g.57788885C= GRCh38
NC_000017.10:g.55866246C= , CM000679.1:g.55866246C= GRCh37
NC_000017.9:g.53221245C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16689G=
XR_934881.3:n.3815-16689G=