Canonical Allele Identifier: CA514475143

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960698G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564651G>C , CM000684.2:g.36564651G>C	GRCh38
NC_000022.10:g.36960698G>C , CM000684.1:g.36960698G>C	GRCh37
NC_000022.9:g.35290644G>C	NCBI36
NG_031861.1:g.142993C>G
NG_031861.2:g.143208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.672C>G MANE Select	ENSP00000300105.6:p.Thr224=
ENST00000300105.6:c.672C>G	ENSP00000300105.6:p.Thr224=
NM_006078.3:c.672C>G	NP_006069.1:p.Thr224=
NM_006078.4:c.672C>G	NP_006069.1:p.Thr224=
XM_017028531.2:c.414C>G	XP_016884020.1:p.Thr138=
NM_001379051.1:c.603C>G	NP_001365980.1:p.Thr201=
NM_006078.5:c.672C>G MANE Select	NP_006069.1:p.Thr224=
NR_166440.1:n.2038C>G