Canonical Allele Identifier: CA2403994155

Gene: CACNG2

Linked Data

• dbSNP Id: rs1601463951

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36701451A>C , CM000684.2:g.36701451A>C	GRCh38
NC_000022.10:g.37097496A>C , CM000684.1:g.37097496A>C	GRCh37
NC_000022.9:g.35427442A>C	NCBI36
NG_031861.1:g.6195T>G
NG_031861.2:g.6408T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.211+915T>G MANE Select	ENSP00000300105.6:n.211+915T>G
ENST00000300105.6:c.211+915T>G	ENSP00000300105.6:n.211+915T>G
NM_006078.3:c.211+915T>G	NP_006069.1:n.211+915T>G
NM_006078.4:c.211+915T>G	NP_006069.1:n.211+915T>G
NM_001379051.1:c.142+915T>G	NP_001365980.1:n.142+915T>G
NM_006078.5:c.211+915T>G MANE Select	NP_006069.1:n.211+915T>G
NR_166440.1:n.1387+915T>G