Canonical Allele Identifier: CA323997928

Gene: CACNG2

Linked Data

• dbSNP Id: rs1023689319
• gnomAD v3: 22-36564964-C-A
• gnomAD v4: 22-36564964-C-A
• MyVariant Identifiers: chr22:g.36961011C>A (hg19) ; chr22:g.36564964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564964C>A , CM000684.2:g.36564964C>A	GRCh38
NC_000022.10:g.36961011C>A , CM000684.1:g.36961011C>A	GRCh37
NC_000022.9:g.35290957C>A	NCBI36
NG_031861.1:g.142680G>T
NG_031861.2:g.142895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-78G>T MANE Select	ENSP00000300105.6:n.437-78G>T
ENST00000300105.6:c.437-78G>T	ENSP00000300105.6:n.437-78G>T
NM_006078.3:c.437-78G>T	NP_006069.1:n.437-78G>T
NM_006078.4:c.437-78G>T	NP_006069.1:n.437-78G>T
XM_017028531.2:c.179-78G>T	XP_016884020.1:n.179-78G>T
NM_001379051.1:c.368-78G>T	NP_001365980.1:n.368-78G>T
NM_006078.5:c.437-78G>T MANE Select	NP_006069.1:n.437-78G>T
NR_166440.1:n.1803-78G>T