Canonical Allele Identifier: CA2403929657
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564717G= , CM000684.2:g.36564717G= GRCh38
NC_000022.10:g.36960764G= , CM000684.1:g.36960764G= GRCh37
NC_000022.9:g.35290710G= NCBI36
NG_031861.1:g.142927C=
NG_031861.2:g.143142C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.606C= MANE Select ENSP00000300105.6:p.Ile202=
ENST00000300105.6:c.606C= ENSP00000300105.6:p.Ile202=
NM_006078.3:c.606C= NP_006069.1:p.Ile202=
NM_006078.4:c.606C= NP_006069.1:p.Ile202=
XM_017028531.2:c.348C= XP_016884020.1:p.Ile116=
NM_001379051.1:c.537C= NP_001365980.1:p.Ile179=
NM_006078.5:c.606C= MANE Select NP_006069.1:p.Ile202=
NR_166440.1:n.1972C=