Canonical Allele Identifier: CA1677669
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs755363481
gnomAD v2: 2-61605585-G-A
gnomAD v4: 2-61378450-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378450G>A , CM000664.2:g.61378450G>A GRCh38
NC_000002.11:g.61605585G>A , CM000664.1:g.61605585G>A GRCh37
NC_000002.10:g.61459089G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-26C>T MANE Select ENSP00000381577.2:n.1015-26C>T
ENST00000398571.6:c.1015-26C>T ENSP00000381577.2:n.1015-26C>T
ENST00000453133.1:c.541-26C>T
NM_014709.3:c.1015-26C>T NP_055524.3:n.1015-26C>T
NM_014709.4:c.1015-26C>T MANE Select NP_055524.3:n.1015-26C>T