Canonical Allele Identifier: CA2403929653
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564711C= , CM000684.2:g.36564711C= GRCh38
NC_000022.10:g.36960758C= , CM000684.1:g.36960758C= GRCh37
NC_000022.9:g.35290704C= NCBI36
NG_031861.1:g.142933G=
NG_031861.2:g.143148G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.612G= MANE Select ENSP00000300105.6:p.Arg204=
ENST00000300105.6:c.612G= ENSP00000300105.6:p.Arg204=
NM_006078.3:c.612G= NP_006069.1:p.Arg204=
NM_006078.4:c.612G= NP_006069.1:p.Arg204=
XM_017028531.2:c.354G= XP_016884020.1:p.Arg118=
NM_001379051.1:c.543G= NP_001365980.1:p.Arg181=
NM_006078.5:c.612G= MANE Select NP_006069.1:p.Arg204=
NR_166440.1:n.1978G=