Canonical Allele Identifier: CA48428847
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs948902042
gnomAD v3: 2-61378517-T-C
gnomAD v4: 2-61378517-T-C
MyVariant Identifiers: chr2:g.61605652T>C (hg19) chr2:g.61378517T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378517T>C , CM000664.2:g.61378517T>C GRCh38
NC_000002.11:g.61605652T>C , CM000664.1:g.61605652T>C GRCh37
NC_000002.10:g.61459156T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-93A>G MANE Select ENSP00000381577.2:n.1015-93A>G
ENST00000398571.6:c.1015-93A>G ENSP00000381577.2:n.1015-93A>G
ENST00000453133.1:c.541-93A>G
NM_014709.3:c.1015-93A>G NP_055524.3:n.1015-93A>G
NM_014709.4:c.1015-93A>G MANE Select NP_055524.3:n.1015-93A>G
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