Canonical Allele Identifier: CA450339150

Gene: UBR2

Linked Data

• MyVariant Identifiers: chr6:g.42561973T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42594235T>C , CM000668.2:g.42594235T>C	GRCh38
NC_000006.11:g.42561973T>C , CM000668.1:g.42561973T>C	GRCh37
NC_000006.10:g.42669951T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372899.6:c.462T>C	ENSP00000361990.1:p.Thr154=
ENST00000372901.2:c.462T>C MANE Select	ENSP00000361992.1:p.Thr154=
ENST00000372899.5:c.462T>C	ENSP00000361990.1:p.Thr154=
ENST00000372901.1:c.462T>C	ENSP00000361992.1:p.Thr154=
ENST00000372903.6:c.462T>C	ENSP00000361994.2:p.Thr154=
NM_001184801.1:c.462T>C	NP_001171730.1:p.Thr154=
NM_015255.2:c.462T>C	NP_056070.1:p.Thr154=
XM_005248965.3:c.462T>C	XP_005249022.1:p.Thr154=
XM_011514438.1:c.276T>C	XP_011512740.1:p.Thr92=
XM_011514442.1:c.462T>C	XP_011512744.1:p.Thr154=
NM_001363705.1:c.462T>C	NP_001350634.1:p.Thr154=
XM_005248966.3:c.-1644T>C	XP_005249023.1:n.-1644T>C
XM_011514438.2:c.543T>C	XP_011512740.2:p.Thr181=
XM_017010594.1:c.543T>C	XP_016866083.1:p.Thr181=
XM_017010595.1:c.543T>C	XP_016866084.1:p.Thr181=
XM_017010596.1:c.462T>C	XP_016866085.1:p.Thr154=
XM_017010597.1:c.543T>C	XP_016866086.1:p.Thr181=
XR_001743284.2:n.961T>C
XR_001743285.1:n.962T>C
NM_001184801.2:c.462T>C	NP_001171730.1:p.Thr154=
NM_001363705.2:c.462T>C MANE Select	NP_001350634.1:p.Thr154=
NM_015255.3:c.462T>C	NP_056070.1:p.Thr154=