Canonical Allele Identifier: CA346974597
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1245357995
gnomAD v2: 2-61605534-A-C
gnomAD v4: 2-61378399-A-C
MyVariant Identifiers: chr2:g.61605534A>C (hg19) chr2:g.61378399A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378399A>C , CM000664.2:g.61378399A>C GRCh38
NC_000002.11:g.61605534A>C , CM000664.1:g.61605534A>C GRCh37
NC_000002.10:g.61459038A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1040T>G MANE Select ENSP00000381577.2:p.Val347Gly
ENST00000398571.6:c.1040T>G ENSP00000381577.2:p.Val347Gly
ENST00000453133.1:c.566T>G
NM_014709.3:c.1040T>G NP_055524.3:p.Val347Gly
NM_014709.4:c.1040T>G MANE Select NP_055524.3:p.Val347Gly
Search 100 bp 5'
Search 100 bp 3'