Canonical Allele Identifier: CA48428567

Gene: USP34

Linked Data

• dbSNP Id: rs1013622401
• gnomAD v3: 2-61378311-C-T
• gnomAD v4: 2-61378311-C-T
• MyVariant Identifiers: chr2:g.61605446C>T (hg19) ; chr2:g.61378311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378311C>T , CM000664.2:g.61378311C>T	GRCh38
NC_000002.11:g.61605446C>T , CM000664.1:g.61605446C>T	GRCh37
NC_000002.10:g.61458950C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+52G>A MANE Select	ENSP00000381577.2:n.1076+52G>A
ENST00000398571.6:c.1076+52G>A	ENSP00000381577.2:n.1076+52G>A
ENST00000453133.1:c.602+52G>A
NM_014709.3:c.1076+52G>A	NP_055524.3:n.1076+52G>A
NM_014709.4:c.1076+52G>A MANE Select	NP_055524.3:n.1076+52G>A