Canonical Allele Identifier: CA1406123012
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1935183983
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528281C>T , CM000665.2:g.140528281C>T GRCh38
NC_000003.11:g.140247123C>T , CM000665.1:g.140247123C>T GRCh37
NC_000003.10:g.141729813C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.1345-4043C>T MANE Select ENSP00000402460.2:n.1345-4043C>T
ENST00000511524.1:n.1533-4043C>T
ENST00000620185.1:c.1153-4043C>T ENSP00000478883.1:n.1153-4043C>T
NM_022131.2:c.1345-4043C>T NP_071414.2:n.1345-4043C>T
XM_017007022.2:c.1270-4043C>T XP_016862511.1:n.1270-4043C>T
NM_022131.3:c.1345-4043C>T MANE Select NP_071414.2:n.1345-4043C>T
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