Canonical Allele Identifier: CA48428924
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1000281308
MyVariant Identifiers: chr2:g.61605700A>T (hg19) chr2:g.61378565A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378565A>T , CM000664.2:g.61378565A>T GRCh38
NC_000002.11:g.61605700A>T , CM000664.1:g.61605700A>T GRCh37
NC_000002.10:g.61459204A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-141T>A MANE Select ENSP00000381577.2:n.1015-141T>A
ENST00000398571.6:c.1015-141T>A ENSP00000381577.2:n.1015-141T>A
ENST00000453133.1:c.541-141T>A
NM_014709.3:c.1015-141T>A NP_055524.3:n.1015-141T>A
NM_014709.4:c.1015-141T>A MANE Select NP_055524.3:n.1015-141T>A
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