Canonical Allele Identifier: CA323997966
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs980879264
gnomAD v2: 22-36961049-C-T
gnomAD v3: 22-36565002-C-T
gnomAD v4: 22-36565002-C-T
MyVariant Identifiers: chr22:g.36961049C>T (hg19) chr22:g.36565002C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36565002C>T , CM000684.2:g.36565002C>T GRCh38
NC_000022.10:g.36961049C>T , CM000684.1:g.36961049C>T GRCh37
NC_000022.9:g.35290995C>T NCBI36
NG_031861.1:g.142642G>A
NG_031861.2:g.142857G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-116G>A MANE Select ENSP00000300105.6:n.437-116G>A
ENST00000300105.6:c.437-116G>A ENSP00000300105.6:n.437-116G>A
NM_006078.3:c.437-116G>A NP_006069.1:n.437-116G>A
NM_006078.4:c.437-116G>A NP_006069.1:n.437-116G>A
XM_017028531.2:c.179-116G>A XP_016884020.1:n.179-116G>A
NM_001379051.1:c.368-116G>A NP_001365980.1:n.368-116G>A
NM_006078.5:c.437-116G>A MANE Select NP_006069.1:n.437-116G>A
NR_166440.1:n.1803-116G>A
Search 100 bp 5'
Search 100 bp 3'