Canonical Allele Identifier: CA617631785
Gene: UBR1 HGNC NCBI

Linked Data

dbSNP Id: rs1223875516

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42957917A>G , CM000677.2:g.42957917A>G GRCh38
NC_000015.9:g.43250115A>G , CM000677.1:g.43250115A>G GRCh37
NC_000015.8:g.41037407A>G NCBI36
NG_012182.1:g.153172T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4835+96T>C MANE Select ENSP00000290650.4:n.4835+96T>C
ENST00000290650.8:c.4835+96T>C ENSP00000290650.4:n.4835+96T>C
NM_174916.2:c.4835+96T>C NP_777576.1:n.4835+96T>C
NM_174916.3:c.4835+96T>C MANE Select NP_777576.1:n.4835+96T>C