Canonical Allele Identifier: CA411377818

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960846G>C (hg19) ; chr22:g.36564799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564799G>C , CM000684.2:g.36564799G>C	GRCh38
NC_000022.10:g.36960846G>C , CM000684.1:g.36960846G>C	GRCh37
NC_000022.9:g.35290792G>C	NCBI36
NG_031861.1:g.142845C>G
NG_031861.2:g.143060C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.524C>G MANE Select	ENSP00000300105.6:p.Ser175Ter
ENST00000300105.6:c.524C>G	ENSP00000300105.6:p.Ser175Ter
NM_006078.3:c.524C>G	NP_006069.1:p.Ser175Ter
NM_006078.4:c.524C>G	NP_006069.1:p.Ser175Ter
XM_017028531.2:c.266C>G	XP_016884020.1:p.Ser89Ter
NM_001379051.1:c.455C>G	NP_001365980.1:p.Ser152Ter
NM_006078.5:c.524C>G MANE Select	NP_006069.1:p.Ser175Ter
NR_166440.1:n.1890C>G