Canonical Allele Identifier: CA2172970089
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958123A= , CM000677.2:g.42958123A= GRCh38
NC_000015.9:g.43250321A= , CM000677.1:g.43250321A= GRCh37
NC_000015.8:g.41037613A= NCBI36
NG_012182.1:g.152966T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-33T= MANE Select ENSP00000290650.4:n.4758-33T=
ENST00000290650.8:c.4758-33T= ENSP00000290650.4:n.4758-33T=
NM_174916.2:c.4758-33T= NP_777576.1:n.4758-33T=
NM_174916.3:c.4758-33T= MANE Select NP_777576.1:n.4758-33T=