Canonical Allele Identifier: CA426205611
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605518T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378383T>A , CM000664.2:g.61378383T>A GRCh38
NC_000002.11:g.61605518T>A , CM000664.1:g.61605518T>A GRCh37
NC_000002.10:g.61459022T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1056A>T MANE Select ENSP00000381577.2:p.Ser352=
ENST00000398571.6:c.1056A>T ENSP00000381577.2:p.Ser352=
ENST00000453133.1:c.582A>T
NM_014709.3:c.1056A>T NP_055524.3:p.Ser352=
NM_014709.4:c.1056A>T MANE Select NP_055524.3:p.Ser352=
Search 100 bp 5'
Search 100 bp 3'