Canonical Allele Identifier: CA514475121

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960887G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564840G>C , CM000684.2:g.36564840G>C	GRCh38
NC_000022.10:g.36960887G>C , CM000684.1:g.36960887G>C	GRCh37
NC_000022.9:g.35290833G>C	NCBI36
NG_031861.1:g.142804C>G
NG_031861.2:g.143019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.483C>G MANE Select	ENSP00000300105.6:p.Ala161=
ENST00000300105.6:c.483C>G	ENSP00000300105.6:p.Ala161=
NM_006078.3:c.483C>G	NP_006069.1:p.Ala161=
NM_006078.4:c.483C>G	NP_006069.1:p.Ala161=
XM_017028531.2:c.225C>G	XP_016884020.1:p.Ala75=
NM_001379051.1:c.414C>G	NP_001365980.1:p.Ala138=
NM_006078.5:c.483C>G MANE Select	NP_006069.1:p.Ala161=
NR_166440.1:n.1849C>G