Canonical Allele Identifier: CA25557348

Gene: PRKACB

Linked Data

• dbSNP Id: rs1021162815
• MyVariant Identifiers: chr1:g.84566661T>C (hg19) ; chr1:g.84100978T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84100978T>C , CM000663.2:g.84100978T>C	GRCh38
NC_000001.10:g.84566661T>C , CM000663.1:g.84566661T>C	GRCh37
NC_000001.9:g.84339249T>C	NCBI36
NG_029728.1:g.27917T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370688.7:c.46+22607T>C	ENSP00000359722.3:n.46+22607T>C
ENST00000370689.6:c.46+22607T>C	ENSP00000359723.2:n.46+22607T>C
NM_002731.3:c.46+22607T>C	NP_002722.1:n.46+22607T>C
NM_207578.2:c.46+22607T>C	NP_997461.1:n.46+22607T>C
XM_011541764.1:c.46+22607T>C	XP_011540066.1:n.46+22607T>C
XM_017001713.2:c.46+22607T>C	XP_016857202.1:n.46+22607T>C
NM_001375576.1:c.46+22607T>C	NP_001362505.1:n.46+22607T>C
NM_207578.3:c.46+22607T>C	NP_997461.1:n.46+22607T>C
NM_002731.4:c.46+22607T>C	NP_002722.1:n.46+22607T>C