Canonical Allele Identifier: CA2172970229
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958267T= , CM000677.2:g.42958267T= GRCh38
NC_000015.9:g.43250465T= , CM000677.1:g.43250465T= GRCh37
NC_000015.8:g.41037757T= NCBI36
NG_012182.1:g.152822A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-177A= MANE Select ENSP00000290650.4:n.4758-177A=
ENST00000290650.8:c.4758-177A= ENSP00000290650.4:n.4758-177A=
NM_174916.2:c.4758-177A= NP_777576.1:n.4758-177A=
NM_174916.3:c.4758-177A= MANE Select NP_777576.1:n.4758-177A=