Canonical Allele Identifier: CA2172970174
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958188G= , CM000677.2:g.42958188G= GRCh38
NC_000015.9:g.43250386G= , CM000677.1:g.43250386G= GRCh37
NC_000015.8:g.41037678G= NCBI36
NG_012182.1:g.152901C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-98C= MANE Select ENSP00000290650.4:n.4758-98C=
ENST00000290650.8:c.4758-98C= ENSP00000290650.4:n.4758-98C=
NM_174916.2:c.4758-98C= NP_777576.1:n.4758-98C=
NM_174916.3:c.4758-98C= MANE Select NP_777576.1:n.4758-98C=