Canonical Allele Identifier: CA1677658
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs764100584
ExAC: 2:61605531 C / T
gnomAD v2: 2-61605531-C-T
gnomAD v4: 2-61378396-C-T
MyVariant Identifiers: chr2:g.61605531C>T (hg19) chr2:g.61378396C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378396C>T , CM000664.2:g.61378396C>T GRCh38
NC_000002.11:g.61605531C>T , CM000664.1:g.61605531C>T GRCh37
NC_000002.10:g.61459035C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1043G>A MANE Select ENSP00000381577.2:p.Cys348Tyr
ENST00000398571.6:c.1043G>A ENSP00000381577.2:p.Cys348Tyr
ENST00000453133.1:c.569G>A
NM_014709.3:c.1043G>A NP_055524.3:p.Cys348Tyr
NM_014709.4:c.1043G>A MANE Select NP_055524.3:p.Cys348Tyr
Search 100 bp 5'
Search 100 bp 3'