Canonical Allele Identifier: CA346974549
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1262790189
gnomAD v2: 2-61605525-T-C
gnomAD v4: 2-61378390-T-C
MyVariant Identifiers: chr2:g.61605525T>C (hg19) chr2:g.61378390T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378390T>C , CM000664.2:g.61378390T>C GRCh38
NC_000002.11:g.61605525T>C , CM000664.1:g.61605525T>C GRCh37
NC_000002.10:g.61459029T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1049A>G MANE Select ENSP00000381577.2:p.Asn350Ser
ENST00000398571.6:c.1049A>G ENSP00000381577.2:p.Asn350Ser
ENST00000453133.1:c.575A>G
NM_014709.3:c.1049A>G NP_055524.3:p.Asn350Ser
NM_014709.4:c.1049A>G MANE Select NP_055524.3:p.Asn350Ser
Search 100 bp 5'
Search 100 bp 3'