Canonical Allele Identifier: CA2403929770
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1603500174
gnomAD v4: 22-36565005-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36565005G>C , CM000684.2:g.36565005G>C GRCh38
NC_000022.10:g.36961052G>C , CM000684.1:g.36961052G>C GRCh37
NC_000022.9:g.35290998G>C NCBI36
NG_031861.1:g.142639C>G
NG_031861.2:g.142854C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-119C>G MANE Select ENSP00000300105.6:n.437-119C>G
ENST00000300105.6:c.437-119C>G ENSP00000300105.6:n.437-119C>G
NM_006078.3:c.437-119C>G NP_006069.1:n.437-119C>G
NM_006078.4:c.437-119C>G NP_006069.1:n.437-119C>G
XM_017028531.2:c.179-119C>G XP_016884020.1:n.179-119C>G
NM_001379051.1:c.368-119C>G NP_001365980.1:n.368-119C>G
NM_006078.5:c.437-119C>G MANE Select NP_006069.1:n.437-119C>G
NR_166440.1:n.1803-119C>G
Search 100 bp 5'
Search 100 bp 3'