Canonical Allele Identifier: CA411377661

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960829A>C (hg19) ; chr22:g.36564782A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564782A>C , CM000684.2:g.36564782A>C	GRCh38
NC_000022.10:g.36960829A>C , CM000684.1:g.36960829A>C	GRCh37
NC_000022.9:g.35290775A>C	NCBI36
NG_031861.1:g.142862T>G
NG_031861.2:g.143077T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.541T>G MANE Select	ENSP00000300105.6:p.Tyr181Asp
ENST00000300105.6:c.541T>G	ENSP00000300105.6:p.Tyr181Asp
NM_006078.3:c.541T>G	NP_006069.1:p.Tyr181Asp
NM_006078.4:c.541T>G	NP_006069.1:p.Tyr181Asp
XM_017028531.2:c.283T>G	XP_016884020.1:p.Tyr95Asp
NM_001379051.1:c.472T>G	NP_001365980.1:p.Tyr158Asp
NM_006078.5:c.541T>G MANE Select	NP_006069.1:p.Tyr181Asp
NR_166440.1:n.1907T>G