Canonical Allele Identifier: CA1405859369
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1935539719
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139963123T>G , CM000665.2:g.139963123T>G GRCh38
NC_000003.11:g.139681965T>G , CM000665.1:g.139681965T>G GRCh37
NC_000003.10:g.141164655T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.109+27640T>G MANE Select ENSP00000402460.2:n.109+27640T>G
ENST00000511524.1:n.297+27640T>G
NM_022131.2:c.109+27640T>G NP_071414.2:n.109+27640T>G
NM_022131.3:c.109+27640T>G MANE Select NP_071414.2:n.109+27640T>G
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