Canonical Allele Identifier: CA2269954628
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506298A= , CM000679.2:g.63506298A= GRCh38
NC_000017.10:g.61583659A= , CM000679.1:g.61583659A= GRCh37
NC_000017.9:g.58937391A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-758A= ENSP00000464149.1:n.1970-758A=