Canonical Allele Identifier: CA2269954656
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506367A= , CM000679.2:g.63506367A= GRCh38
NC_000017.10:g.61583728A= , CM000679.1:g.61583728A= GRCh37
NC_000017.9:g.58937460A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-689A= ENSP00000464149.1:n.1970-689A=