Canonical Allele Identifier: CA514475090

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960656G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564609G>A , CM000684.2:g.36564609G>A	GRCh38
NC_000022.10:g.36960656G>A , CM000684.1:g.36960656G>A	GRCh37
NC_000022.9:g.35290602G>A	NCBI36
NG_031861.1:g.143035C>T
NG_031861.2:g.143250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.714C>T MANE Select	ENSP00000300105.6:p.Arg238=
ENST00000300105.6:c.714C>T	ENSP00000300105.6:p.Arg238=
NM_006078.3:c.714C>T	NP_006069.1:p.Arg238=
NM_006078.4:c.714C>T	NP_006069.1:p.Arg238=
XM_017028531.2:c.456C>T	XP_016884020.1:p.Arg152=
NM_001379051.1:c.645C>T	NP_001365980.1:p.Arg215=
NM_006078.5:c.714C>T MANE Select	NP_006069.1:p.Arg238=
NR_166440.1:n.2080C>T