Canonical Allele Identifier: CA514475147

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960905C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564858C>G , CM000684.2:g.36564858C>G	GRCh38
NC_000022.10:g.36960905C>G , CM000684.1:g.36960905C>G	GRCh37
NC_000022.9:g.35290851C>G	NCBI36
NG_031861.1:g.142786G>C
NG_031861.2:g.143001G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.465G>C MANE Select	ENSP00000300105.6:p.Val155=
ENST00000300105.6:c.465G>C	ENSP00000300105.6:p.Val155=
NM_006078.3:c.465G>C	NP_006069.1:p.Val155=
NM_006078.4:c.465G>C	NP_006069.1:p.Val155=
XM_017028531.2:c.207G>C	XP_016884020.1:p.Val69=
NM_001379051.1:c.396G>C	NP_001365980.1:p.Val132=
NM_006078.5:c.465G>C MANE Select	NP_006069.1:p.Val155=
NR_166440.1:n.1831G>C