Canonical Allele Identifier: CA2269954639
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506328G= , CM000679.2:g.63506328G= GRCh38
NC_000017.10:g.61583689G= , CM000679.1:g.61583689G= GRCh37
NC_000017.9:g.58937421G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-728G= ENSP00000464149.1:n.1970-728G=