Canonical Allele Identifier: CA739632756

Gene: PRKACB

Linked Data

• dbSNP Id: rs1420494669
• MyVariant Identifiers: chr1:g.84566611C>T (hg19) ; chr1:g.84100928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84100928C>T , CM000663.2:g.84100928C>T	GRCh38
NC_000001.10:g.84566611C>T , CM000663.1:g.84566611C>T	GRCh37
NC_000001.9:g.84339199C>T	NCBI36
NG_029728.1:g.27867C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370688.7:c.46+22557C>T	ENSP00000359722.3:n.46+22557C>T
ENST00000370689.6:c.46+22557C>T	ENSP00000359723.2:n.46+22557C>T
NM_002731.3:c.46+22557C>T	NP_002722.1:n.46+22557C>T
NM_207578.2:c.46+22557C>T	NP_997461.1:n.46+22557C>T
XM_011541764.1:c.46+22557C>T	XP_011540066.1:n.46+22557C>T
XM_017001713.2:c.46+22557C>T	XP_016857202.1:n.46+22557C>T
NM_001375576.1:c.46+22557C>T	NP_001362505.1:n.46+22557C>T
NM_207578.3:c.46+22557C>T	NP_997461.1:n.46+22557C>T
NM_002731.4:c.46+22557C>T	NP_002722.1:n.46+22557C>T