Canonical Allele Identifier: CA2263926900
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211664C= , CM000679.2:g.50211664C= GRCh38
NC_000017.10:g.48289025C= , CM000679.1:g.48289025C= GRCh37
NC_000017.9:g.45644024C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2171C=