Canonical Allele Identifier: CA2267413199
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788895T= , CM000679.2:g.57788895T= GRCh38
NC_000017.10:g.55866256T= , CM000679.1:g.55866256T= GRCh37
NC_000017.9:g.53221255T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16699A=
XR_934881.3:n.3815-16699A=