Canonical Allele Identifier: CA411377610

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960823C>A (hg19) ; chr22:g.36564776C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564776C>A , CM000684.2:g.36564776C>A	GRCh38
NC_000022.10:g.36960823C>A , CM000684.1:g.36960823C>A	GRCh37
NC_000022.9:g.35290769C>A	NCBI36
NG_031861.1:g.142868G>T
NG_031861.2:g.143083G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.547G>T MANE Select	ENSP00000300105.6:p.Gly183Trp
ENST00000300105.6:c.547G>T	ENSP00000300105.6:p.Gly183Trp
NM_006078.3:c.547G>T	NP_006069.1:p.Gly183Trp
NM_006078.4:c.547G>T	NP_006069.1:p.Gly183Trp
XM_017028531.2:c.289G>T	XP_016884020.1:p.Gly97Trp
NM_001379051.1:c.478G>T	NP_001365980.1:p.Gly160Trp
NM_006078.5:c.547G>T MANE Select	NP_006069.1:p.Gly183Trp
NR_166440.1:n.1913G>T