Canonical Allele Identifier: CA392058205
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43250290T>C (hg19) chr15:g.42958092T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958092T>C , CM000677.2:g.42958092T>C GRCh38
NC_000015.9:g.43250290T>C , CM000677.1:g.43250290T>C GRCh37
NC_000015.8:g.41037582T>C NCBI36
NG_012182.1:g.152997A>G

Transcript Alleles

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