Canonical Allele Identifier: CA2267413198
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788887C= , CM000679.2:g.57788887C= GRCh38
NC_000017.10:g.55866248C= , CM000679.1:g.55866248C= GRCh37
NC_000017.9:g.53221247C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16691G=
XR_934881.3:n.3815-16691G=