Canonical Allele Identifier: CA411377672
Gene: CACNG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564784A>C , CM000684.2:g.36564784A>C GRCh38
NC_000022.10:g.36960831A>C , CM000684.1:g.36960831A>C GRCh37
NC_000022.9:g.35290777A>C NCBI36
NG_031861.1:g.142860T>G
NG_031861.2:g.143075T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.539T>G MANE Select ENSP00000300105.6:p.Phe180Cys
ENST00000300105.6:c.539T>G ENSP00000300105.6:p.Phe180Cys
NM_006078.3:c.539T>G NP_006069.1:p.Phe180Cys
NM_006078.4:c.539T>G NP_006069.1:p.Phe180Cys
XM_017028531.2:c.281T>G XP_016884020.1:p.Phe94Cys
NM_001379051.1:c.470T>G NP_001365980.1:p.Phe157Cys
NM_006078.5:c.539T>G MANE Select NP_006069.1:p.Phe180Cys
NR_166440.1:n.1905T>G