Canonical Allele Identifier: CA532842436
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1255492286
gnomAD v2: 2-61605610-G-C
gnomAD v4: 2-61378475-G-C
MyVariant Identifiers: chr2:g.61605610G>C (hg19) chr2:g.61378475G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378475G>C , CM000664.2:g.61378475G>C GRCh38
NC_000002.11:g.61605610G>C , CM000664.1:g.61605610G>C GRCh37
NC_000002.10:g.61459114G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-51C>G MANE Select ENSP00000381577.2:n.1015-51C>G
ENST00000398571.6:c.1015-51C>G ENSP00000381577.2:n.1015-51C>G
ENST00000453133.1:c.541-51C>G
NM_014709.3:c.1015-51C>G NP_055524.3:n.1015-51C>G
NM_014709.4:c.1015-51C>G MANE Select NP_055524.3:n.1015-51C>G
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