Canonical Allele Identifier: CA770955655
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1421645486
gnomAD v3: 2-61378265-T-A
gnomAD v4: 2-61378265-T-A
MyVariant Identifiers: chr2:g.61605400T>A (hg19) chr2:g.61378265T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378265T>A , CM000664.2:g.61378265T>A GRCh38
NC_000002.11:g.61605400T>A , CM000664.1:g.61605400T>A GRCh37
NC_000002.10:g.61458904T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+98A>T MANE Select ENSP00000381577.2:n.1076+98A>T
ENST00000398571.6:c.1076+98A>T ENSP00000381577.2:n.1076+98A>T
ENST00000453133.1:c.602+98A>T
NM_014709.3:c.1076+98A>T NP_055524.3:n.1076+98A>T
NM_014709.4:c.1076+98A>T MANE Select NP_055524.3:n.1076+98A>T
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