Canonical Allele Identifier: CA2403929641
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564686G= , CM000684.2:g.36564686G= GRCh38
NC_000022.10:g.36960733G= , CM000684.1:g.36960733G= GRCh37
NC_000022.9:g.35290679G= NCBI36
NG_031861.1:g.142958C=
NG_031861.2:g.143173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.637C= MANE Select ENSP00000300105.6:p.Arg213=
ENST00000300105.6:c.637C= ENSP00000300105.6:p.Arg213=
NM_006078.3:c.637C= NP_006069.1:p.Arg213=
NM_006078.4:c.637C= NP_006069.1:p.Arg213=
XM_017028531.2:c.379C= XP_016884020.1:p.Arg127=
NM_001379051.1:c.568C= NP_001365980.1:p.Arg190=
NM_006078.5:c.637C= MANE Select NP_006069.1:p.Arg213=
NR_166440.1:n.2003C=