Canonical Allele Identifier: CA532842381

Gene: USP34

Linked Data

• dbSNP Id: rs1414423344
• gnomAD v2: 2-61605475-T-C
• gnomAD v4: 2-61378340-T-C
• MyVariant Identifiers: chr2:g.61605475T>C (hg19) ; chr2:g.61378340T>C (hg38)

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