Canonical Allele Identifier: CA770955609
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs970534178
gnomAD v3: 2-61378158-G-T
gnomAD v4: 2-61378158-G-T
MyVariant Identifiers: chr2:g.61605293G>T (hg19) chr2:g.61378158G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378158G>T , CM000664.2:g.61378158G>T GRCh38
NC_000002.11:g.61605293G>T , CM000664.1:g.61605293G>T GRCh37
NC_000002.10:g.61458797G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+205C>A MANE Select ENSP00000381577.2:n.1076+205C>A
ENST00000398571.6:c.1076+205C>A ENSP00000381577.2:n.1076+205C>A
ENST00000453133.1:c.602+205C>A
NM_014709.3:c.1076+205C>A NP_055524.3:n.1076+205C>A
NM_014709.4:c.1076+205C>A MANE Select NP_055524.3:n.1076+205C>A
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