Canonical Allele Identifier: CA2242459483
Community Standard Title: NC_000017.11:g.715725T=
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.715725T= , CM000679.2:g.715725T= GRCh38
NC_000017.10:g.618965T= , CM000679.1:g.618965T= GRCh37
NC_000017.9:g.565715T= NCBI36
NG_034190.1:g.4132A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000576019.5:c.-282-5112A= ENSP00000461429.1:n.-282-5112A=
ENST00000680704.1:c.-282-5112A= ENSP00000506453.1:n.-282-5112A=