Canonical Allele Identifier: CA346974516
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1692859495
gnomAD v3: 2-61378387-T-A
gnomAD v4: 2-61378387-T-A
MyVariant Identifiers: chr2:g.61605522T>A (hg19) chr2:g.61378387T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378387T>A , CM000664.2:g.61378387T>A GRCh38
NC_000002.11:g.61605522T>A , CM000664.1:g.61605522T>A GRCh37
NC_000002.10:g.61459026T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1052A>T MANE Select ENSP00000381577.2:p.Glu351Val
ENST00000398571.6:c.1052A>T ENSP00000381577.2:p.Glu351Val
ENST00000453133.1:c.578A>T
NM_014709.3:c.1052A>T NP_055524.3:p.Glu351Val
NM_014709.4:c.1052A>T MANE Select NP_055524.3:p.Glu351Val
Search 100 bp 5'
Search 100 bp 3'