Canonical Allele Identifier: CA1301166063
Community Standard Title: NC_000002.12:g.157923692G=
Gene: UPP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.157923692G= , CM000664.2:g.157923692G= GRCh38
NC_000002.11:g.158780204G= , CM000664.1:g.158780204G= GRCh37
NC_000002.10:g.158488450G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000605860.5:c.-20+46964G= ENSP00000474090.1:n.-20+46964G=