Canonical Allele Identifier: CA411376706

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960699G>C (hg19) ; chr22:g.36564652G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564652G>C , CM000684.2:g.36564652G>C	GRCh38
NC_000022.10:g.36960699G>C , CM000684.1:g.36960699G>C	GRCh37
NC_000022.9:g.35290645G>C	NCBI36
NG_031861.1:g.142992C>G
NG_031861.2:g.143207C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.671C>G MANE Select	ENSP00000300105.6:p.Thr224Ser
ENST00000300105.6:c.671C>G	ENSP00000300105.6:p.Thr224Ser
NM_006078.3:c.671C>G	NP_006069.1:p.Thr224Ser
NM_006078.4:c.671C>G	NP_006069.1:p.Thr224Ser
XM_017028531.2:c.413C>G	XP_016884020.1:p.Thr138Ser
NM_001379051.1:c.602C>G	NP_001365980.1:p.Thr201Ser
NM_006078.5:c.671C>G MANE Select	NP_006069.1:p.Thr224Ser
NR_166440.1:n.2037C>G