Canonical Allele Identifier: CA346974641
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1436099811
gnomAD v2: 2-61605544-A-C
gnomAD v4: 2-61378409-A-C
MyVariant Identifiers: chr2:g.61605544A>C (hg19) chr2:g.61378409A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378409A>C , CM000664.2:g.61378409A>C GRCh38
NC_000002.11:g.61605544A>C , CM000664.1:g.61605544A>C GRCh37
NC_000002.10:g.61459048A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1030T>G MANE Select ENSP00000381577.2:p.Phe344Val
ENST00000398571.6:c.1030T>G ENSP00000381577.2:p.Phe344Val
ENST00000453133.1:c.556T>G
NM_014709.3:c.1030T>G NP_055524.3:p.Phe344Val
NM_014709.4:c.1030T>G MANE Select NP_055524.3:p.Phe344Val
Search 100 bp 5'
Search 100 bp 3'