Canonical Allele Identifier: CA514475172

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960920G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564873G>T , CM000684.2:g.36564873G>T	GRCh38
NC_000022.10:g.36960920G>T , CM000684.1:g.36960920G>T	GRCh37
NC_000022.9:g.35290866G>T	NCBI36
NG_031861.1:g.142771C>A
NG_031861.2:g.142986C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.450C>A MANE Select	ENSP00000300105.6:p.Ile150=
ENST00000300105.6:c.450C>A	ENSP00000300105.6:p.Ile150=
NM_006078.3:c.450C>A	NP_006069.1:p.Ile150=
NM_006078.4:c.450C>A	NP_006069.1:p.Ile150=
XM_017028531.2:c.192C>A	XP_016884020.1:p.Ile64=
NM_001379051.1:c.381C>A	NP_001365980.1:p.Ile127=
NM_006078.5:c.450C>A MANE Select	NP_006069.1:p.Ile150=
NR_166440.1:n.1816C>A