Canonical Allele Identifier: CA392080606
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43360217T>C (hg19) chr15:g.43068019T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43068019T>C , CM000677.2:g.43068019T>C GRCh38
NC_000015.9:g.43360217T>C , CM000677.1:g.43360217T>C GRCh37
NC_000015.8:g.41147509T>C NCBI36
NG_012182.1:g.43070A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.677A>G MANE Select ENSP00000290650.4:p.Tyr226Cys
ENST00000290650.8:c.677A>G ENSP00000290650.4:p.Tyr226Cys
ENST00000546274.6:c.677A>G ENSP00000477932.1:p.Tyr226Cys
ENST00000563239.1:c.*202+2880A>G ENSP00000456502.1:n.*202+2880A>G
NM_174916.2:c.677A>G NP_777576.1:p.Tyr226Cys
NM_174916.3:c.677A>G MANE Select NP_777576.1:p.Tyr226Cys
Search 100 bp 5'
Search 100 bp 3'