Canonical Allele Identifier: CA532842381
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1414423344
gnomAD v2: 2-61605475-T-C
gnomAD v4: 2-61378340-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378340T>C , CM000664.2:g.61378340T>C GRCh38
NC_000002.11:g.61605475T>C , CM000664.1:g.61605475T>C GRCh37
NC_000002.10:g.61458979T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+23A>G MANE Select ENSP00000381577.2:n.1076+23A>G
ENST00000398571.6:c.1076+23A>G ENSP00000381577.2:n.1076+23A>G
ENST00000453133.1:c.602+23A>G
NM_014709.3:c.1076+23A>G NP_055524.3:n.1076+23A>G
NM_014709.4:c.1076+23A>G MANE Select NP_055524.3:n.1076+23A>G