Canonical Allele Identifier: CA2269954631
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506305G= , CM000679.2:g.63506305G= GRCh38
NC_000017.10:g.61583666G= , CM000679.1:g.61583666G= GRCh37
NC_000017.9:g.58937398G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-751G= ENSP00000464149.1:n.1970-751G=