Canonical Allele Identifier: CA489907270
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43250258C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958060C>T , CM000677.2:g.42958060C>T GRCh38
NC_000015.9:g.43250258C>T , CM000677.1:g.43250258C>T GRCh37
NC_000015.8:g.41037550C>T NCBI36
NG_012182.1:g.153029G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4788G>A MANE Select ENSP00000290650.4:p.Glu1596=
ENST00000290650.8:c.4788G>A ENSP00000290650.4:p.Glu1596=
NM_174916.2:c.4788G>A NP_777576.1:p.Glu1596=
NM_174916.3:c.4788G>A MANE Select NP_777576.1:p.Glu1596=
Search 100 bp 5'
Search 100 bp 3'