Canonical Allele Identifier: CA138412808
Gene: UBR2 HGNC NCBI

Linked Data

dbSNP Id: rs9381199
gnomAD v4: 6-42594234-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42594234C>T , CM000668.2:g.42594234C>T GRCh38
NC_000006.11:g.42561972C>T , CM000668.1:g.42561972C>T GRCh37
NC_000006.10:g.42669950C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000372899.6:c.461C>T ENSP00000361990.1:p.Thr154Ile
ENST00000372901.2:c.461C>T MANE Select ENSP00000361992.1:p.Thr154Ile
ENST00000372899.5:c.461C>T ENSP00000361990.1:p.Thr154Ile
ENST00000372901.1:c.461C>T ENSP00000361992.1:p.Thr154Ile
ENST00000372903.6:c.461C>T ENSP00000361994.2:p.Thr154Ile
NM_001184801.1:c.461C>T NP_001171730.1:p.Thr154Ile
NM_015255.2:c.461C>T NP_056070.1:p.Thr154Ile
XM_005248965.3:c.461C>T XP_005249022.1:p.Thr154Ile
XM_011514438.1:c.275C>T XP_011512740.1:p.Thr92Ile
XM_011514442.1:c.461C>T XP_011512744.1:p.Thr154Ile
NM_001363705.1:c.461C>T NP_001350634.1:p.Thr154Ile
XM_005248966.3:c.-1645C>T XP_005249023.1:n.-1645C>T
XM_011514438.2:c.542C>T XP_011512740.2:p.Thr181Ile
XM_017010594.1:c.542C>T XP_016866083.1:p.Thr181Ile
XM_017010595.1:c.542C>T XP_016866084.1:p.Thr181Ile
XM_017010596.1:c.461C>T XP_016866085.1:p.Thr154Ile
XM_017010597.1:c.542C>T XP_016866086.1:p.Thr181Ile
XR_001743284.2:n.960C>T
XR_001743285.1:n.961C>T
NM_001184801.2:c.461C>T NP_001171730.1:p.Thr154Ile
NM_001363705.2:c.461C>T MANE Select NP_001350634.1:p.Thr154Ile
NM_015255.3:c.461C>T NP_056070.1:p.Thr154Ile