Canonical Allele Identifier: CA1180310417
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs1571578762

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100850T>C , CM000663.2:g.84100850T>C GRCh38
NC_000001.10:g.84566533T>C , CM000663.1:g.84566533T>C GRCh37
NC_000001.9:g.84339121T>C NCBI36
NG_029728.1:g.27789T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370688.7:c.46+22479T>C ENSP00000359722.3:n.46+22479T>C
ENST00000370689.6:c.46+22479T>C ENSP00000359723.2:n.46+22479T>C
NM_002731.3:c.46+22479T>C NP_002722.1:n.46+22479T>C
NM_207578.2:c.46+22479T>C NP_997461.1:n.46+22479T>C
XM_011541764.1:c.46+22479T>C XP_011540066.1:n.46+22479T>C
XM_017001713.2:c.46+22479T>C XP_016857202.1:n.46+22479T>C
NM_001375576.1:c.46+22479T>C NP_001362505.1:n.46+22479T>C
NM_207578.3:c.46+22479T>C NP_997461.1:n.46+22479T>C
NM_002731.4:c.46+22479T>C NP_002722.1:n.46+22479T>C