Canonical Allele Identifier: CA2699522232
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs2103857000
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378264T>A , CM000664.2:g.61378264T>A GRCh38
NC_000002.11:g.61605399T>A , CM000664.1:g.61605399T>A GRCh37
NC_000002.10:g.61458903T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+99A>T MANE Select ENSP00000381577.2:n.1076+99A>T
ENST00000398571.6:c.1076+99A>T ENSP00000381577.2:n.1076+99A>T
ENST00000453133.1:c.602+99A>T
NM_014709.3:c.1076+99A>T NP_055524.3:n.1076+99A>T
NM_014709.4:c.1076+99A>T MANE Select NP_055524.3:n.1076+99A>T
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