Canonical Allele Identifier: CA899761633
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1474570942

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528357C>A , CM000665.2:g.140528357C>A GRCh38
NC_000003.11:g.140247199C>A , CM000665.1:g.140247199C>A GRCh37
NC_000003.10:g.141729889C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-3967C>A MANE Select ENSP00000402460.2:n.1345-3967C>A
ENST00000511524.1:n.1533-3967C>A
ENST00000620185.1:c.1153-3967C>A ENSP00000478883.1:n.1153-3967C>A
NM_022131.2:c.1345-3967C>A NP_071414.2:n.1345-3967C>A
XM_017007022.2:c.1270-3967C>A XP_016862511.1:n.1270-3967C>A
NM_022131.3:c.1345-3967C>A MANE Select NP_071414.2:n.1345-3967C>A