Canonical Allele Identifier: CA752858040

Gene: CACNG2

Linked Data

• dbSNP Id: rs543280827
• gnomAD v4: 22-36564965-G-T
• MyVariant Identifiers: chr22:g.36961012G>T (hg19) ; chr22:g.36564965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564965G>T , CM000684.2:g.36564965G>T	GRCh38
NC_000022.10:g.36961012G>T , CM000684.1:g.36961012G>T	GRCh37
NC_000022.9:g.35290958G>T	NCBI36
NG_031861.1:g.142679C>A
NG_031861.2:g.142894C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-79C>A MANE Select	ENSP00000300105.6:n.437-79C>A
ENST00000300105.6:c.437-79C>A	ENSP00000300105.6:n.437-79C>A
NM_006078.3:c.437-79C>A	NP_006069.1:n.437-79C>A
NM_006078.4:c.437-79C>A	NP_006069.1:n.437-79C>A
XM_017028531.2:c.179-79C>A	XP_016884020.1:n.179-79C>A
NM_001379051.1:c.368-79C>A	NP_001365980.1:n.368-79C>A
NM_006078.5:c.437-79C>A MANE Select	NP_006069.1:n.437-79C>A
NR_166440.1:n.1803-79C>A