Canonical Allele Identifier: CA737669212
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs1288434363
gnomAD v3: 1-62447593-G-A
gnomAD v4: 1-62447593-G-A
MyVariant Identifiers: chr1:g.62913264G>A (hg19) chr1:g.62447593G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447593G>A , CM000663.2:g.62447593G>A GRCh38
NC_000001.10:g.62913264G>A , CM000663.1:g.62913264G>A GRCh37
NC_000001.9:g.62685852G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1420+82G>A MANE Select ENSP00000343526.4:n.1420+82G>A
ENST00000339950.4:c.1420+82G>A ENSP00000343526.4:n.1420+82G>A
ENST00000371146.5:c.1420+82G>A ENSP00000360188.1:n.1420+82G>A
NM_001017415.1:c.1420+82G>A NP_001017415.1:n.1420+82G>A
NM_001017416.1:c.1420+82G>A NP_001017416.1:n.1420+82G>A
NM_003368.4:c.1420+82G>A NP_003359.3:n.1420+82G>A
NM_003368.5:c.1420+82G>A MANE Select NP_003359.3:n.1420+82G>A
NM_001017415.2:c.1420+82G>A NP_001017415.1:n.1420+82G>A
NM_001017416.2:c.1420+82G>A NP_001017416.1:n.1420+82G>A
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