Canonical Allele Identifier: CA2263926927
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211714C= , CM000679.2:g.50211714C= GRCh38
NC_000017.10:g.48289075C= , CM000679.1:g.48289075C= GRCh37
NC_000017.9:g.45644074C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2121C=