Canonical Allele Identifier: CA346974427
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605506G>C (hg19) chr2:g.61378371G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378371G>C , CM000664.2:g.61378371G>C GRCh38
NC_000002.11:g.61605506G>C , CM000664.1:g.61605506G>C GRCh37
NC_000002.10:g.61459010G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1068C>G MANE Select ENSP00000381577.2:p.Asp356Glu
ENST00000398571.6:c.1068C>G ENSP00000381577.2:p.Asp356Glu
ENST00000453133.1:c.594C>G
NM_014709.3:c.1068C>G NP_055524.3:p.Asp356Glu
NM_014709.4:c.1068C>G MANE Select NP_055524.3:p.Asp356Glu
Search 100 bp 5'
Search 100 bp 3'