Canonical Allele Identifier: CA514475194

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960743C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564696C>A , CM000684.2:g.36564696C>A	GRCh38
NC_000022.10:g.36960743C>A , CM000684.1:g.36960743C>A	GRCh37
NC_000022.9:g.35290689C>A	NCBI36
NG_031861.1:g.142948G>T
NG_031861.2:g.143163G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.627G>T MANE Select	ENSP00000300105.6:p.Arg209=
ENST00000300105.6:c.627G>T	ENSP00000300105.6:p.Arg209=
NM_006078.3:c.627G>T	NP_006069.1:p.Arg209=
NM_006078.4:c.627G>T	NP_006069.1:p.Arg209=
XM_017028531.2:c.369G>T	XP_016884020.1:p.Arg123=
NM_001379051.1:c.558G>T	NP_001365980.1:p.Arg186=
NM_006078.5:c.627G>T MANE Select	NP_006069.1:p.Arg209=
NR_166440.1:n.1993G>T