Canonical Allele Identifier: CA770955946
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1308415999
gnomAD v3: 2-61378484-A-C
gnomAD v4: 2-61378484-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378484A>C , CM000664.2:g.61378484A>C GRCh38
NC_000002.11:g.61605619A>C , CM000664.1:g.61605619A>C GRCh37
NC_000002.10:g.61459123A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-60T>G MANE Select ENSP00000381577.2:n.1015-60T>G
ENST00000398571.6:c.1015-60T>G ENSP00000381577.2:n.1015-60T>G
ENST00000453133.1:c.541-60T>G
NM_014709.3:c.1015-60T>G NP_055524.3:n.1015-60T>G
NM_014709.4:c.1015-60T>G MANE Select NP_055524.3:n.1015-60T>G