Canonical Allele Identifier: CA770955962
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1315829472
gnomAD v3: 2-61378499-G-A
gnomAD v4: 2-61378499-G-A
MyVariant Identifiers: chr2:g.61605634G>A (hg19) chr2:g.61378499G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378499G>A , CM000664.2:g.61378499G>A GRCh38
NC_000002.11:g.61605634G>A , CM000664.1:g.61605634G>A GRCh37
NC_000002.10:g.61459138G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-75C>T MANE Select ENSP00000381577.2:n.1015-75C>T
ENST00000398571.6:c.1015-75C>T ENSP00000381577.2:n.1015-75C>T
ENST00000453133.1:c.541-75C>T
NM_014709.3:c.1015-75C>T NP_055524.3:n.1015-75C>T
NM_014709.4:c.1015-75C>T MANE Select NP_055524.3:n.1015-75C>T
Search 100 bp 5'
Search 100 bp 3'