Canonical Allele Identifier: CA2656451708
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564982-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564982C>G , CM000684.2:g.36564982C>G GRCh38
NC_000022.10:g.36961029C>G , CM000684.1:g.36961029C>G GRCh37
NC_000022.9:g.35290975C>G NCBI36
NG_031861.1:g.142662G>C
NG_031861.2:g.142877G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-96G>C MANE Select ENSP00000300105.6:n.437-96G>C
ENST00000300105.6:c.437-96G>C ENSP00000300105.6:n.437-96G>C
NM_006078.3:c.437-96G>C NP_006069.1:n.437-96G>C
NM_006078.4:c.437-96G>C NP_006069.1:n.437-96G>C
XM_017028531.2:c.179-96G>C XP_016884020.1:n.179-96G>C
NM_001379051.1:c.368-96G>C NP_001365980.1:n.368-96G>C
NM_006078.5:c.437-96G>C MANE Select NP_006069.1:n.437-96G>C
NR_166440.1:n.1803-96G>C
Search 100 bp 5'
Search 100 bp 3'