Canonical Allele Identifier: CA411377871
Gene: CACNG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564803A>T , CM000684.2:g.36564803A>T GRCh38
NC_000022.10:g.36960850A>T , CM000684.1:g.36960850A>T GRCh37
NC_000022.9:g.35290796A>T NCBI36
NG_031861.1:g.142841T>A
NG_031861.2:g.143056T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.520T>A MANE Select ENSP00000300105.6:p.Tyr174Asn
ENST00000300105.6:c.520T>A ENSP00000300105.6:p.Tyr174Asn
NM_006078.3:c.520T>A NP_006069.1:p.Tyr174Asn
NM_006078.4:c.520T>A NP_006069.1:p.Tyr174Asn
XM_017028531.2:c.262T>A XP_016884020.1:p.Tyr88Asn
NM_001379051.1:c.451T>A NP_001365980.1:p.Tyr151Asn
NM_006078.5:c.520T>A MANE Select NP_006069.1:p.Tyr174Asn
NR_166440.1:n.1886T>A