Canonical Allele Identifier: CA323997968

Gene: CACNG2

Linked Data

• dbSNP Id: rs757434574
• gnomAD v4: 22-36565004-C-G
• MyVariant Identifiers: chr22:g.36565004C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36565004C>G , CM000684.2:g.36565004C>G	GRCh38
NC_000022.10:g.36961051C>G , CM000684.1:g.36961051C>G	GRCh37
NC_000022.9:g.35290997C>G	NCBI36
NG_031861.1:g.142640G>C
NG_031861.2:g.142855G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-118G>C MANE Select	ENSP00000300105.6:n.437-118G>C
ENST00000300105.6:c.437-118G>C	ENSP00000300105.6:n.437-118G>C
NM_006078.3:c.437-118G>C	NP_006069.1:n.437-118G>C
NM_006078.4:c.437-118G>C	NP_006069.1:n.437-118G>C
XM_017028531.2:c.179-118G>C	XP_016884020.1:n.179-118G>C
NM_001379051.1:c.368-118G>C	NP_001365980.1:n.368-118G>C
NM_006078.5:c.437-118G>C MANE Select	NP_006069.1:n.437-118G>C
NR_166440.1:n.1803-118G>C