Canonical Allele Identifier: CA514475246

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960818G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564771G>C , CM000684.2:g.36564771G>C	GRCh38
NC_000022.10:g.36960818G>C , CM000684.1:g.36960818G>C	GRCh37
NC_000022.9:g.35290764G>C	NCBI36
NG_031861.1:g.142873C>G
NG_031861.2:g.143088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.552C>G MANE Select	ENSP00000300105.6:p.Ala184=
ENST00000300105.6:c.552C>G	ENSP00000300105.6:p.Ala184=
NM_006078.3:c.552C>G	NP_006069.1:p.Ala184=
NM_006078.4:c.552C>G	NP_006069.1:p.Ala184=
XM_017028531.2:c.294C>G	XP_016884020.1:p.Ala98=
NM_001379051.1:c.483C>G	NP_001365980.1:p.Ala161=
NM_006078.5:c.552C>G MANE Select	NP_006069.1:p.Ala184=
NR_166440.1:n.1918C>G