Canonical Allele Identifier: CA426205622
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378407-G-A
MyVariant Identifiers: chr2:g.61605542G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378407G>A , CM000664.2:g.61378407G>A GRCh38
NC_000002.11:g.61605542G>A , CM000664.1:g.61605542G>A GRCh37
NC_000002.10:g.61459046G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1032C>T MANE Select ENSP00000381577.2:p.Phe344=
ENST00000398571.6:c.1032C>T ENSP00000381577.2:p.Phe344=
ENST00000453133.1:c.558C>T
NM_014709.3:c.1032C>T NP_055524.3:p.Phe344=
NM_014709.4:c.1032C>T MANE Select NP_055524.3:p.Phe344=
Search 100 bp 5'
Search 100 bp 3'