Canonical Allele Identifier: CA48428466
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1000385973
gnomAD v3: 2-61378116-T-A
gnomAD v4: 2-61378116-T-A
MyVariant Identifiers: chr2:g.61605251T>A (hg19) chr2:g.61378116T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378116T>A , CM000664.2:g.61378116T>A GRCh38
NC_000002.11:g.61605251T>A , CM000664.1:g.61605251T>A GRCh37
NC_000002.10:g.61458755T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+247A>T MANE Select ENSP00000381577.2:n.1076+247A>T
ENST00000398571.6:c.1076+247A>T ENSP00000381577.2:n.1076+247A>T
ENST00000453133.1:c.602+247A>T
NM_014709.3:c.1076+247A>T NP_055524.3:n.1076+247A>T
NM_014709.4:c.1076+247A>T MANE Select NP_055524.3:n.1076+247A>T
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