Canonical Allele Identifier: CA346974586
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605529T>C (hg19) chr2:g.61378394T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378394T>C , CM000664.2:g.61378394T>C GRCh38
NC_000002.11:g.61605529T>C , CM000664.1:g.61605529T>C GRCh37
NC_000002.10:g.61459033T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1045A>G MANE Select ENSP00000381577.2:p.Asn349Asp
ENST00000398571.6:c.1045A>G ENSP00000381577.2:p.Asn349Asp
ENST00000453133.1:c.571A>G
NM_014709.3:c.1045A>G NP_055524.3:p.Asn349Asp
NM_014709.4:c.1045A>G MANE Select NP_055524.3:p.Asn349Asp
Search 100 bp 5'
Search 100 bp 3'