Canonical Allele Identifier: CA426205618
Gene: USP34 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61605533C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378398C>G , CM000664.2:g.61378398C>G GRCh38
NC_000002.11:g.61605533C>G , CM000664.1:g.61605533C>G GRCh37
NC_000002.10:g.61459037C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1041G>C MANE Select ENSP00000381577.2:p.Val347=
ENST00000398571.6:c.1041G>C ENSP00000381577.2:p.Val347=
ENST00000453133.1:c.567G>C
NM_014709.3:c.1041G>C NP_055524.3:p.Val347=
NM_014709.4:c.1041G>C MANE Select NP_055524.3:p.Val347=
Search 100 bp 5'
Search 100 bp 3'