Canonical Allele Identifier: CA523754848

Gene: PRKACB

Linked Data

• dbSNP Id: rs1251830881
• gnomAD v2: 1-84566621-T-G
• gnomAD v3: 1-84100938-T-G
• gnomAD v4: 1-84100938-T-G
• MyVariant Identifiers: chr1:g.84566621T>G (hg19) ; chr1:g.84100938T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84100938T>G , CM000663.2:g.84100938T>G	GRCh38
NC_000001.10:g.84566621T>G , CM000663.1:g.84566621T>G	GRCh37
NC_000001.9:g.84339209T>G	NCBI36
NG_029728.1:g.27877T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370688.7:c.46+22567T>G	ENSP00000359722.3:n.46+22567T>G
ENST00000370689.6:c.46+22567T>G	ENSP00000359723.2:n.46+22567T>G
NM_002731.3:c.46+22567T>G	NP_002722.1:n.46+22567T>G
NM_207578.2:c.46+22567T>G	NP_997461.1:n.46+22567T>G
XM_011541764.1:c.46+22567T>G	XP_011540066.1:n.46+22567T>G
XM_017001713.2:c.46+22567T>G	XP_016857202.1:n.46+22567T>G
NM_001375576.1:c.46+22567T>G	NP_001362505.1:n.46+22567T>G
NM_207578.3:c.46+22567T>G	NP_997461.1:n.46+22567T>G
NM_002731.4:c.46+22567T>G	NP_002722.1:n.46+22567T>G