Canonical Allele Identifier: CA2172970079
Gene: UBR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958110G= , CM000677.2:g.42958110G= GRCh38
NC_000015.9:g.43250308G= , CM000677.1:g.43250308G= GRCh37
NC_000015.8:g.41037600G= NCBI36
NG_012182.1:g.152979C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-20C= MANE Select ENSP00000290650.4:n.4758-20C=
ENST00000290650.8:c.4758-20C= ENSP00000290650.4:n.4758-20C=
NM_174916.2:c.4758-20C= NP_777576.1:n.4758-20C=
NM_174916.3:c.4758-20C= MANE Select NP_777576.1:n.4758-20C=
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