Canonical Allele Identifier: CA411376467

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960678T>C (hg19) ; chr22:g.36564631T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564631T>C , CM000684.2:g.36564631T>C	GRCh38
NC_000022.10:g.36960678T>C , CM000684.1:g.36960678T>C	GRCh37
NC_000022.9:g.35290624T>C	NCBI36
NG_031861.1:g.143013A>G
NG_031861.2:g.143228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.692A>G MANE Select	ENSP00000300105.6:p.Tyr231Cys
ENST00000300105.6:c.692A>G	ENSP00000300105.6:p.Tyr231Cys
NM_006078.3:c.692A>G	NP_006069.1:p.Tyr231Cys
NM_006078.4:c.692A>G	NP_006069.1:p.Tyr231Cys
XM_017028531.2:c.434A>G	XP_016884020.1:p.Tyr145Cys
NM_001379051.1:c.623A>G	NP_001365980.1:p.Tyr208Cys
NM_006078.5:c.692A>G MANE Select	NP_006069.1:p.Tyr231Cys
NR_166440.1:n.2058A>G