Canonical Allele Identifier: CA2263926947
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211766A= , CM000679.2:g.50211766A= GRCh38
NC_000017.10:g.48289127A= , CM000679.1:g.48289127A= GRCh37
NC_000017.9:g.45644126A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2069A=