Canonical Allele Identifier: CA514475130

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960893G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564846G>T , CM000684.2:g.36564846G>T	GRCh38
NC_000022.10:g.36960893G>T , CM000684.1:g.36960893G>T	GRCh37
NC_000022.9:g.35290839G>T	NCBI36
NG_031861.1:g.142798C>A
NG_031861.2:g.143013C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.477C>A MANE Select	ENSP00000300105.6:p.Ala159=
ENST00000300105.6:c.477C>A	ENSP00000300105.6:p.Ala159=
NM_006078.3:c.477C>A	NP_006069.1:p.Ala159=
NM_006078.4:c.477C>A	NP_006069.1:p.Ala159=
XM_017028531.2:c.219C>A	XP_016884020.1:p.Ala73=
NM_001379051.1:c.408C>A	NP_001365980.1:p.Ala136=
NM_006078.5:c.477C>A MANE Select	NP_006069.1:p.Ala159=
NR_166440.1:n.1843C>A