Canonical Allele Identifier: CA1031337543
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1692850286
gnomAD v3: 2-61378140-T-G
gnomAD v4: 2-61378140-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378140T>G , CM000664.2:g.61378140T>G GRCh38
NC_000002.11:g.61605275T>G , CM000664.1:g.61605275T>G GRCh37
NC_000002.10:g.61458779T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+223A>C MANE Select ENSP00000381577.2:n.1076+223A>C
ENST00000398571.6:c.1076+223A>C ENSP00000381577.2:n.1076+223A>C
ENST00000453133.1:c.602+223A>C
NM_014709.3:c.1076+223A>C NP_055524.3:n.1076+223A>C
NM_014709.4:c.1076+223A>C MANE Select NP_055524.3:n.1076+223A>C
Search 100 bp 5'
Search 100 bp 3'