Canonical Allele Identifier: CA514475119

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960884T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564837T>C , CM000684.2:g.36564837T>C	GRCh38
NC_000022.10:g.36960884T>C , CM000684.1:g.36960884T>C	GRCh37
NC_000022.9:g.35290830T>C	NCBI36
NG_031861.1:g.142807A>G
NG_031861.2:g.143022A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.486A>G MANE Select	ENSP00000300105.6:p.Gly162=
ENST00000300105.6:c.486A>G	ENSP00000300105.6:p.Gly162=
NM_006078.3:c.486A>G	NP_006069.1:p.Gly162=
NM_006078.4:c.486A>G	NP_006069.1:p.Gly162=
XM_017028531.2:c.228A>G	XP_016884020.1:p.Gly76=
NM_001379051.1:c.417A>G	NP_001365980.1:p.Gly139=
NM_006078.5:c.486A>G MANE Select	NP_006069.1:p.Gly162=
NR_166440.1:n.1852A>G