Canonical Allele Identifier: CA514475155

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960908T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564861T>G , CM000684.2:g.36564861T>G	GRCh38
NC_000022.10:g.36960908T>G , CM000684.1:g.36960908T>G	GRCh37
NC_000022.9:g.35290854T>G	NCBI36
NG_031861.1:g.142783A>C
NG_031861.2:g.142998A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.462A>C MANE Select	ENSP00000300105.6:p.Ile154=
ENST00000300105.6:c.462A>C	ENSP00000300105.6:p.Ile154=
NM_006078.3:c.462A>C	NP_006069.1:p.Ile154=
NM_006078.4:c.462A>C	NP_006069.1:p.Ile154=
XM_017028531.2:c.204A>C	XP_016884020.1:p.Ile68=
NM_001379051.1:c.393A>C	NP_001365980.1:p.Ile131=
NM_006078.5:c.462A>C MANE Select	NP_006069.1:p.Ile154=
NR_166440.1:n.1828A>C