Canonical Allele Identifier: CA770956042

Gene: USP34

Linked Data

• dbSNP Id: rs761275249
• MyVariant Identifiers: chr2:g.61605767G>C (hg19) ; chr2:g.61378632G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378632G>C , CM000664.2:g.61378632G>C	GRCh38
NC_000002.11:g.61605767G>C , CM000664.1:g.61605767G>C	GRCh37
NC_000002.10:g.61459271G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1015-208C>G MANE Select	ENSP00000381577.2:n.1015-208C>G
ENST00000398571.6:c.1015-208C>G	ENSP00000381577.2:n.1015-208C>G
ENST00000453133.1:c.541-208C>G
NM_014709.3:c.1015-208C>G	NP_055524.3:n.1015-208C>G
NM_014709.4:c.1015-208C>G MANE Select	NP_055524.3:n.1015-208C>G