Canonical Allele Identifier: CA346974496
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605519G>C (hg19) chr2:g.61378384G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378384G>C , CM000664.2:g.61378384G>C GRCh38
NC_000002.11:g.61605519G>C , CM000664.1:g.61605519G>C GRCh37
NC_000002.10:g.61459023G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1055C>G MANE Select ENSP00000381577.2:p.Ser352Ter
ENST00000398571.6:c.1055C>G ENSP00000381577.2:p.Ser352Ter
ENST00000453133.1:c.581C>G
NM_014709.3:c.1055C>G NP_055524.3:p.Ser352Ter
NM_014709.4:c.1055C>G MANE Select NP_055524.3:p.Ser352Ter
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