Canonical Allele Identifier: CA514475226

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960788C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564741C>A , CM000684.2:g.36564741C>A	GRCh38
NC_000022.10:g.36960788C>A , CM000684.1:g.36960788C>A	GRCh37
NC_000022.9:g.35290734C>A	NCBI36
NG_031861.1:g.142903G>T
NG_031861.2:g.143118G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.582G>T MANE Select	ENSP00000300105.6:p.Gly194=
ENST00000300105.6:c.582G>T	ENSP00000300105.6:p.Gly194=
NM_006078.3:c.582G>T	NP_006069.1:p.Gly194=
NM_006078.4:c.582G>T	NP_006069.1:p.Gly194=
XM_017028531.2:c.324G>T	XP_016884020.1:p.Gly108=
NM_001379051.1:c.513G>T	NP_001365980.1:p.Gly171=
NM_006078.5:c.582G>T MANE Select	NP_006069.1:p.Gly194=
NR_166440.1:n.1948G>T