Canonical Allele Identifier: CA514475100

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960665G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564618G>C , CM000684.2:g.36564618G>C	GRCh38
NC_000022.10:g.36960665G>C , CM000684.1:g.36960665G>C	GRCh37
NC_000022.9:g.35290611G>C	NCBI36
NG_031861.1:g.143026C>G
NG_031861.2:g.143241C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.705C>G MANE Select	ENSP00000300105.6:p.Arg235=
ENST00000300105.6:c.705C>G	ENSP00000300105.6:p.Arg235=
NM_006078.3:c.705C>G	NP_006069.1:p.Arg235=
NM_006078.4:c.705C>G	NP_006069.1:p.Arg235=
XM_017028531.2:c.447C>G	XP_016884020.1:p.Arg149=
NM_001379051.1:c.636C>G	NP_001365980.1:p.Arg212=
NM_006078.5:c.705C>G MANE Select	NP_006069.1:p.Arg235=
NR_166440.1:n.2071C>G