Canonical Allele Identifier: CA770955592
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1352428607
gnomAD v3: 2-61378127-C-T
gnomAD v4: 2-61378127-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378127C>T , CM000664.2:g.61378127C>T GRCh38
NC_000002.11:g.61605262C>T , CM000664.1:g.61605262C>T GRCh37
NC_000002.10:g.61458766C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+236G>A MANE Select ENSP00000381577.2:n.1076+236G>A
ENST00000398571.6:c.1076+236G>A ENSP00000381577.2:n.1076+236G>A
ENST00000453133.1:c.602+236G>A
NM_014709.3:c.1076+236G>A NP_055524.3:n.1076+236G>A
NM_014709.4:c.1076+236G>A MANE Select NP_055524.3:n.1076+236G>A