Canonical Allele Identifier: CA1677661
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs767050787
ExAC: 2:61605569 A / C
gnomAD v2: 2-61605569-A-C
gnomAD v3: 2-61378434-A-C
gnomAD v4: 2-61378434-A-C
MyVariant Identifiers: chr2:g.61605569A>C (hg19) chr2:g.61378434A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378434A>C , CM000664.2:g.61378434A>C GRCh38
NC_000002.11:g.61605569A>C , CM000664.1:g.61605569A>C GRCh37
NC_000002.10:g.61459073A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-10T>G MANE Select ENSP00000381577.2:n.1015-10T>G
ENST00000398571.6:c.1015-10T>G ENSP00000381577.2:n.1015-10T>G
ENST00000453133.1:c.541-10T>G
NM_014709.3:c.1015-10T>G NP_055524.3:n.1015-10T>G
NM_014709.4:c.1015-10T>G MANE Select NP_055524.3:n.1015-10T>G
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