Canonical Allele Identifier: CA2656451714

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564987-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564987T>C , CM000684.2:g.36564987T>C	GRCh38
NC_000022.10:g.36961034T>C , CM000684.1:g.36961034T>C	GRCh37
NC_000022.9:g.35290980T>C	NCBI36
NG_031861.1:g.142657A>G
NG_031861.2:g.142872A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-101A>G MANE Select	ENSP00000300105.6:n.437-101A>G
ENST00000300105.6:c.437-101A>G	ENSP00000300105.6:n.437-101A>G
NM_006078.3:c.437-101A>G	NP_006069.1:n.437-101A>G
NM_006078.4:c.437-101A>G	NP_006069.1:n.437-101A>G
XM_017028531.2:c.179-101A>G	XP_016884020.1:n.179-101A>G
NM_001379051.1:c.368-101A>G	NP_001365980.1:n.368-101A>G
NM_006078.5:c.437-101A>G MANE Select	NP_006069.1:n.437-101A>G
NR_166440.1:n.1803-101A>G