Canonical Allele Identifier: CA490121023
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43360123C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43067925C>T , CM000677.2:g.43067925C>T GRCh38
NC_000015.9:g.43360123C>T , CM000677.1:g.43360123C>T GRCh37
NC_000015.8:g.41147415C>T NCBI36
NG_012182.1:g.43164G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.771G>A MANE Select ENSP00000290650.4:p.Gln257=
ENST00000290650.8:c.771G>A ENSP00000290650.4:p.Gln257=
ENST00000546274.6:c.771G>A ENSP00000477932.1:p.Gln257=
ENST00000563239.1:c.*202+2974G>A ENSP00000456502.1:n.*202+2974G>A
NM_174916.2:c.771G>A NP_777576.1:p.Gln257=
NM_174916.3:c.771G>A MANE Select NP_777576.1:p.Gln257=
Search 100 bp 5'
Search 100 bp 3'