Canonical Allele Identifier: CA1003892028
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs1649297022
gnomAD v3: 1-84100822-A-G
gnomAD v4: 1-84100822-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100822A>G , CM000663.2:g.84100822A>G GRCh38
NC_000001.10:g.84566505A>G , CM000663.1:g.84566505A>G GRCh37
NC_000001.9:g.84339093A>G NCBI36
NG_029728.1:g.27761A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370688.7:c.46+22451A>G ENSP00000359722.3:n.46+22451A>G
ENST00000370689.6:c.46+22451A>G ENSP00000359723.2:n.46+22451A>G
NM_002731.3:c.46+22451A>G NP_002722.1:n.46+22451A>G
NM_207578.2:c.46+22451A>G NP_997461.1:n.46+22451A>G
XM_011541764.1:c.46+22451A>G XP_011540066.1:n.46+22451A>G
XM_017001713.2:c.46+22451A>G XP_016857202.1:n.46+22451A>G
NM_001375576.1:c.46+22451A>G NP_001362505.1:n.46+22451A>G
NM_207578.3:c.46+22451A>G NP_997461.1:n.46+22451A>G
NM_002731.4:c.46+22451A>G NP_002722.1:n.46+22451A>G