Canonical Allele Identifier: CA2269954676
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506412A= , CM000679.2:g.63506412A= GRCh38
NC_000017.10:g.61583773A= , CM000679.1:g.61583773A= GRCh37
NC_000017.9:g.58937505A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577647.2:c.1970-644A= ENSP00000464149.1:n.1970-644A=