Canonical Allele Identifier: CA392080669
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43360228T>G (hg19) chr15:g.43068030T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43068030T>G , CM000677.2:g.43068030T>G GRCh38
NC_000015.9:g.43360228T>G , CM000677.1:g.43360228T>G GRCh37
NC_000015.8:g.41147520T>G NCBI36
NG_012182.1:g.43059A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.666A>C MANE Select ENSP00000290650.4:p.Lys222Asn
ENST00000290650.8:c.666A>C ENSP00000290650.4:p.Lys222Asn
ENST00000546274.6:c.666A>C ENSP00000477932.1:p.Lys222Asn
ENST00000563239.1:c.*202+2869A>C ENSP00000456502.1:n.*202+2869A>C
NM_174916.2:c.666A>C NP_777576.1:p.Lys222Asn
NM_174916.3:c.666A>C MANE Select NP_777576.1:p.Lys222Asn
Search 100 bp 5'
Search 100 bp 3'