Canonical Allele Identifier: CA770955952
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1289496695
gnomAD v3: 2-61378493-T-C
gnomAD v4: 2-61378493-T-C
MyVariant Identifiers: chr2:g.61605628T>C (hg19) chr2:g.61378493T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378493T>C , CM000664.2:g.61378493T>C GRCh38
NC_000002.11:g.61605628T>C , CM000664.1:g.61605628T>C GRCh37
NC_000002.10:g.61459132T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-69A>G MANE Select ENSP00000381577.2:n.1015-69A>G
ENST00000398571.6:c.1015-69A>G ENSP00000381577.2:n.1015-69A>G
ENST00000453133.1:c.541-69A>G
NM_014709.3:c.1015-69A>G NP_055524.3:n.1015-69A>G
NM_014709.4:c.1015-69A>G MANE Select NP_055524.3:n.1015-69A>G
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