Canonical Allele Identifier: CA2403929666
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564747C= , CM000684.2:g.36564747C= GRCh38
NC_000022.10:g.36960794C= , CM000684.1:g.36960794C= GRCh37
NC_000022.9:g.35290740C= NCBI36
NG_031861.1:g.142897G=
NG_031861.2:g.143112G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.576G= MANE Select ENSP00000300105.6:p.Met192=
ENST00000300105.6:c.576G= ENSP00000300105.6:p.Met192=
NM_006078.3:c.576G= NP_006069.1:p.Met192=
NM_006078.4:c.576G= NP_006069.1:p.Met192=
XM_017028531.2:c.318G= XP_016884020.1:p.Met106=
NM_001379051.1:c.507G= NP_001365980.1:p.Met169=
NM_006078.5:c.576G= MANE Select NP_006069.1:p.Met192=
NR_166440.1:n.1942G=