Canonical Allele Identifier: CA411376857

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960717A>G (hg19) ; chr22:g.36564670A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564670A>G , CM000684.2:g.36564670A>G	GRCh38
NC_000022.10:g.36960717A>G , CM000684.1:g.36960717A>G	GRCh37
NC_000022.9:g.35290663A>G	NCBI36
NG_031861.1:g.142974T>C
NG_031861.2:g.143189T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.653T>C MANE Select	ENSP00000300105.6:p.Leu218Pro
ENST00000300105.6:c.653T>C	ENSP00000300105.6:p.Leu218Pro
NM_006078.3:c.653T>C	NP_006069.1:p.Leu218Pro
NM_006078.4:c.653T>C	NP_006069.1:p.Leu218Pro
XM_017028531.2:c.395T>C	XP_016884020.1:p.Leu132Pro
NM_001379051.1:c.584T>C	NP_001365980.1:p.Leu195Pro
NM_006078.5:c.653T>C MANE Select	NP_006069.1:p.Leu218Pro
NR_166440.1:n.2019T>C