Canonical Allele Identifier: CA1180310443
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs1252159830

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100930C>A , CM000663.2:g.84100930C>A GRCh38
NC_000001.10:g.84566613C>A , CM000663.1:g.84566613C>A GRCh37
NC_000001.9:g.84339201C>A NCBI36
NG_029728.1:g.27869C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370688.7:c.46+22559C>A ENSP00000359722.3:n.46+22559C>A
ENST00000370689.6:c.46+22559C>A ENSP00000359723.2:n.46+22559C>A
NM_002731.3:c.46+22559C>A NP_002722.1:n.46+22559C>A
NM_207578.2:c.46+22559C>A NP_997461.1:n.46+22559C>A
XM_011541764.1:c.46+22559C>A XP_011540066.1:n.46+22559C>A
XM_017001713.2:c.46+22559C>A XP_016857202.1:n.46+22559C>A
NM_001375576.1:c.46+22559C>A NP_001362505.1:n.46+22559C>A
NM_207578.3:c.46+22559C>A NP_997461.1:n.46+22559C>A
NM_002731.4:c.46+22559C>A NP_002722.1:n.46+22559C>A