Canonical Allele Identifier: CA2269954652
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506353G= , CM000679.2:g.63506353G= GRCh38
NC_000017.10:g.61583714G= , CM000679.1:g.61583714G= GRCh37
NC_000017.9:g.58937446G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-703G= ENSP00000464149.1:n.1970-703G=