Canonical Allele Identifier: CA84592898
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs538834050
gnomAD v3: 3-140528365-A-G
gnomAD v4: 3-140528365-A-G
MyVariant Identifiers: chr3:g.140247207A>G (hg19) chr3:g.140528365A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528365A>G , CM000665.2:g.140528365A>G GRCh38
NC_000003.11:g.140247207A>G , CM000665.1:g.140247207A>G GRCh37
NC_000003.10:g.141729897A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-3959A>G MANE Select ENSP00000402460.2:n.1345-3959A>G
ENST00000511524.1:n.1533-3959A>G
ENST00000620185.1:c.1153-3959A>G ENSP00000478883.1:n.1153-3959A>G
NM_022131.2:c.1345-3959A>G NP_071414.2:n.1345-3959A>G
XM_017007022.2:c.1270-3959A>G XP_016862511.1:n.1270-3959A>G
NM_022131.3:c.1345-3959A>G MANE Select NP_071414.2:n.1345-3959A>G
Search 100 bp 5'
Search 100 bp 3'