Canonical Allele Identifier: CA2599211542
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs2103857630
gnomAD v3: 2-61378548-A-G
gnomAD v4: 2-61378548-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378548A>G , CM000664.2:g.61378548A>G GRCh38
NC_000002.11:g.61605683A>G , CM000664.1:g.61605683A>G GRCh37
NC_000002.10:g.61459187A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-124T>C MANE Select ENSP00000381577.2:n.1015-124T>C
ENST00000398571.6:c.1015-124T>C ENSP00000381577.2:n.1015-124T>C
ENST00000453133.1:c.541-124T>C
NM_014709.3:c.1015-124T>C NP_055524.3:n.1015-124T>C
NM_014709.4:c.1015-124T>C MANE Select NP_055524.3:n.1015-124T>C