Canonical Allele Identifier: CA346974595
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605532A>G (hg19) chr2:g.61378397A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378397A>G , CM000664.2:g.61378397A>G GRCh38
NC_000002.11:g.61605532A>G , CM000664.1:g.61605532A>G GRCh37
NC_000002.10:g.61459036A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1042T>C MANE Select ENSP00000381577.2:p.Cys348Arg
ENST00000398571.6:c.1042T>C ENSP00000381577.2:p.Cys348Arg
ENST00000453133.1:c.568T>C
NM_014709.3:c.1042T>C NP_055524.3:p.Cys348Arg
NM_014709.4:c.1042T>C MANE Select NP_055524.3:p.Cys348Arg
Search 100 bp 5'
Search 100 bp 3'