Canonical Allele Identifier: CA2454681982
Gene: UPF3B HGNC NCBI

Linked Data

dbSNP Id: rs1603371048

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119843311C>A , CM000685.2:g.119843311C>A GRCh38
NC_000023.10:g.118977274C>A , CM000685.1:g.118977274C>A GRCh37
NC_000023.9:g.118861302C>A NCBI36
NG_009241.1:g.14695G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276201.7:c.470-10G>T MANE Select ENSP00000276201.3:n.470-10G>T
ENST00000276201.6:c.470-10G>T ENSP00000276201.2:n.470-10G>T
ENST00000345865.6:c.470-10G>T ENSP00000245418.2:n.470-10G>T
ENST00000478840.1:n.58-10G>T
ENST00000619445.1:c.470-10G>T ENSP00000481698.1:n.470-10G>T
NM_023010.3:c.470-10G>T NP_075386.1:n.470-10G>T
NM_080632.2:c.470-10G>T NP_542199.1:n.470-10G>T
XM_005262458.3:c.470-10G>T XP_005262515.1:n.470-10G>T
XM_006724780.2:c.470-10G>T XP_006724843.1:n.470-10G>T
XM_006724781.2:c.470-10G>T XP_006724844.1:n.470-10G>T
XM_011531378.1:c.470-10G>T XP_011529680.1:n.470-10G>T
XM_011531379.1:c.470-10G>T XP_011529681.1:n.470-10G>T
XM_017029737.1:c.470-10G>T XP_016885226.1:n.470-10G>T
XM_017029738.1:c.470-10G>T XP_016885227.1:n.470-10G>T
XM_017029739.1:c.470-10G>T XP_016885228.1:n.470-10G>T
XM_017029740.1:c.470-10G>T XP_016885229.1:n.470-10G>T
NM_080632.3:c.470-10G>T MANE Select NP_542199.1:n.470-10G>T
NM_023010.4:c.470-10G>T NP_075386.1:n.470-10G>T