Canonical Allele Identifier: CA269934325
Gene: UBR1 HGNC NCBI

Linked Data

dbSNP Id: rs927421443
gnomAD v2: 15-43250465-T-G
MyVariant Identifiers: chr15:g.43250465T>G (hg19) chr15:g.42958267T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958267T>G , CM000677.2:g.42958267T>G GRCh38
NC_000015.9:g.43250465T>G , CM000677.1:g.43250465T>G GRCh37
NC_000015.8:g.41037757T>G NCBI36
NG_012182.1:g.152822A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-177A>C MANE Select ENSP00000290650.4:n.4758-177A>C
ENST00000290650.8:c.4758-177A>C ENSP00000290650.4:n.4758-177A>C
NM_174916.2:c.4758-177A>C NP_777576.1:n.4758-177A>C
NM_174916.3:c.4758-177A>C MANE Select NP_777576.1:n.4758-177A>C
Search 100 bp 5'
Search 100 bp 3'