Canonical Allele Identifier: CA489907243
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43250219A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958021A>C , CM000677.2:g.42958021A>C GRCh38
NC_000015.9:g.43250219A>C , CM000677.1:g.43250219A>C GRCh37
NC_000015.8:g.41037511A>C NCBI36
NG_012182.1:g.153068T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4827T>G MANE Select ENSP00000290650.4:p.Ser1609=
ENST00000290650.8:c.4827T>G ENSP00000290650.4:p.Ser1609=
NM_174916.2:c.4827T>G NP_777576.1:p.Ser1609=
NM_174916.3:c.4827T>G MANE Select NP_777576.1:p.Ser1609=
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