Canonical Allele Identifier: CA2267413195
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788881A= , CM000679.2:g.57788881A= GRCh38
NC_000017.10:g.55866242A= , CM000679.1:g.55866242A= GRCh37
NC_000017.9:g.53221241A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16685T=
XR_934881.3:n.3815-16685T=