Canonical Allele Identifier: CA1180310442
Gene: PRKACB HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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