Canonical Allele Identifier: CA25557328
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs779007934
MyVariant Identifiers: chr1:g.84566537G>A (hg19) chr1:g.84100854G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100854G>A , CM000663.2:g.84100854G>A GRCh38
NC_000001.10:g.84566537G>A , CM000663.1:g.84566537G>A GRCh37
NC_000001.9:g.84339125G>A NCBI36
NG_029728.1:g.27793G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370688.7:c.46+22483G>A ENSP00000359722.3:n.46+22483G>A
ENST00000370689.6:c.46+22483G>A ENSP00000359723.2:n.46+22483G>A
NM_002731.3:c.46+22483G>A NP_002722.1:n.46+22483G>A
NM_207578.2:c.46+22483G>A NP_997461.1:n.46+22483G>A
XM_011541764.1:c.46+22483G>A XP_011540066.1:n.46+22483G>A
XM_017001713.2:c.46+22483G>A XP_016857202.1:n.46+22483G>A
NM_001375576.1:c.46+22483G>A NP_001362505.1:n.46+22483G>A
NM_207578.3:c.46+22483G>A NP_997461.1:n.46+22483G>A
NM_002731.4:c.46+22483G>A NP_002722.1:n.46+22483G>A
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