Canonical Allele Identifier: CA514475174

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564681-G-A
• MyVariant Identifiers: chr22:g.36960728G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564681G>A , CM000684.2:g.36564681G>A	GRCh38
NC_000022.10:g.36960728G>A , CM000684.1:g.36960728G>A	GRCh37
NC_000022.9:g.35290674G>A	NCBI36
NG_031861.1:g.142963C>T
NG_031861.2:g.143178C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.642C>T MANE Select	ENSP00000300105.6:p.Ala214=
ENST00000300105.6:c.642C>T	ENSP00000300105.6:p.Ala214=
NM_006078.3:c.642C>T	NP_006069.1:p.Ala214=
NM_006078.4:c.642C>T	NP_006069.1:p.Ala214=
XM_017028531.2:c.384C>T	XP_016884020.1:p.Ala128=
NM_001379051.1:c.573C>T	NP_001365980.1:p.Ala191=
NM_006078.5:c.642C>T MANE Select	NP_006069.1:p.Ala214=
NR_166440.1:n.2008C>T