Canonical Allele Identifier: CA2172970097
Gene: UBR1 HGNC NCBI

Linked Data

dbSNP Id: rs2031953649
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958129A>C , CM000677.2:g.42958129A>C GRCh38
NC_000015.9:g.43250327A>C , CM000677.1:g.43250327A>C GRCh37
NC_000015.8:g.41037619A>C NCBI36
NG_012182.1:g.152960T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-39T>G MANE Select ENSP00000290650.4:n.4758-39T>G
ENST00000290650.8:c.4758-39T>G ENSP00000290650.4:n.4758-39T>G
NM_174916.2:c.4758-39T>G NP_777576.1:n.4758-39T>G
NM_174916.3:c.4758-39T>G MANE Select NP_777576.1:n.4758-39T>G
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