Canonical Allele Identifier: CA2656451698

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564972-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564972A>T , CM000684.2:g.36564972A>T	GRCh38
NC_000022.10:g.36961019A>T , CM000684.1:g.36961019A>T	GRCh37
NC_000022.9:g.35290965A>T	NCBI36
NG_031861.1:g.142672T>A
NG_031861.2:g.142887T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-86T>A MANE Select	ENSP00000300105.6:n.437-86T>A
ENST00000300105.6:c.437-86T>A	ENSP00000300105.6:n.437-86T>A
NM_006078.3:c.437-86T>A	NP_006069.1:n.437-86T>A
NM_006078.4:c.437-86T>A	NP_006069.1:n.437-86T>A
XM_017028531.2:c.179-86T>A	XP_016884020.1:n.179-86T>A
NM_001379051.1:c.368-86T>A	NP_001365980.1:n.368-86T>A
NM_006078.5:c.437-86T>A MANE Select	NP_006069.1:n.437-86T>A
NR_166440.1:n.1803-86T>A