Canonical Allele Identifier: CA2269954632
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506306G= , CM000679.2:g.63506306G= GRCh38
NC_000017.10:g.61583667G= , CM000679.1:g.61583667G= GRCh37
NC_000017.9:g.58937399G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-750G= ENSP00000464149.1:n.1970-750G=