Canonical Allele Identifier: CA2656451657

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564920-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564920G>T , CM000684.2:g.36564920G>T	GRCh38
NC_000022.10:g.36960967G>T , CM000684.1:g.36960967G>T	GRCh37
NC_000022.9:g.35290913G>T	NCBI36
NG_031861.1:g.142724C>A
NG_031861.2:g.142939C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-34C>A MANE Select	ENSP00000300105.6:n.437-34C>A
ENST00000300105.6:c.437-34C>A	ENSP00000300105.6:n.437-34C>A
NM_006078.3:c.437-34C>A	NP_006069.1:n.437-34C>A
NM_006078.4:c.437-34C>A	NP_006069.1:n.437-34C>A
XM_017028531.2:c.179-34C>A	XP_016884020.1:n.179-34C>A
NM_001379051.1:c.368-34C>A	NP_001365980.1:n.368-34C>A
NM_006078.5:c.437-34C>A MANE Select	NP_006069.1:n.437-34C>A
NR_166440.1:n.1803-34C>A