Canonical Allele Identifier: CA831152517

Gene: PRKAR2B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107122773G>C , CM000669.2:g.107122773G>C	GRCh38
NC_000007.13:g.106763218G>C , CM000669.1:g.106763218G>C	GRCh37
NC_000007.12:g.106550454G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000488792.2:n.548+769G>C
ENST00000706580.1:n.394+769G>C
ENST00000706581.1:c.156+769G>C	ENSP00000516463.1:n.156+769G>C
ENST00000706582.1:n.209+769G>C
ENST00000706583.1:n.474+769G>C
ENST00000706584.1:n.456+769G>C
ENST00000706585.1:n.418+769G>C
ENST00000706586.1:n.414+769G>C
ENST00000706587.1:n.326+769G>C
ENST00000706588.1:n.210+769G>C
ENST00000265717.5:c.396+769G>C MANE Select	ENSP00000265717.4:n.396+769G>C
ENST00000265717.4:c.396+769G>C	ENSP00000265717.4:n.396+769G>C
ENST00000393613.6:n.451+769G>C
ENST00000488792.1:n.263+769G>C
NM_002736.2:c.396+769G>C	NP_002727.2:n.396+769G>C
XM_011516398.1:c.396+769G>C	XP_011514700.1:n.396+769G>C
XM_011516399.1:c.-91+769G>C	XP_011514701.1:n.-91+769G>C
XM_024446836.1:c.-7+769G>C	XP_024302604.1:n.-7+769G>C
NM_002736.3:c.396+769G>C MANE Select	NP_002727.2:n.396+769G>C