Canonical Allele Identifier: CA2172969988
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958014T= , CM000677.2:g.42958014T= GRCh38
NC_000015.9:g.43250212T= , CM000677.1:g.43250212T= GRCh37
NC_000015.8:g.41037504T= NCBI36
NG_012182.1:g.153075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4834A= MANE Select ENSP00000290650.4:p.Arg1612=
ENST00000290650.8:c.4834A= ENSP00000290650.4:p.Arg1612=
NM_174916.2:c.4834A= NP_777576.1:p.Arg1612=
NM_174916.3:c.4834A= MANE Select NP_777576.1:p.Arg1612=