Canonical Allele Identifier: CA11087662
Gene: UPP2 HGNC NCBI

Linked Data

dbSNP Id: rs10183640

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000605860.5:c.-20+46964G>A ENSP00000474090.1:n.-20+46964G>A