Canonical Allele Identifier: CA1471768185

Gene: PRKG2

Linked Data

• dbSNP Id: rs1753324074

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.81201673T>C , CM000666.2:g.81201673T>C	GRCh38
NC_000004.11:g.82122827T>C , CM000666.1:g.82122827T>C	GRCh37
NC_000004.10:g.82341851T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264399.6:c.461+2914A>G MANE Select	ENSP00000264399.1:n.461+2914A>G
ENST00000264399.5:c.461+2914A>G	ENSP00000264399.1:n.461+2914A>G
ENST00000395578.3:c.461+2914A>G	ENSP00000378945.1:n.461+2914A>G
ENST00000628926.1:c.461+2914A>G	ENSP00000486129.1:n.461+2914A>G
NM_001282485.1:c.461+2914A>G	NP_001269414.1:n.461+2914A>G
NM_006259.2:c.461+2914A>G	NP_006250.1:n.461+2914A>G
XM_005263126.2:c.461+2914A>G	XP_005263183.1:n.461+2914A>G
XM_011532114.1:c.461+2914A>G	XP_011530416.1:n.461+2914A>G
XM_011532115.1:c.461+2914A>G	XP_011530417.1:n.461+2914A>G
XM_011532116.1:c.461+2914A>G	XP_011530418.1:n.461+2914A>G
NM_001363401.1:c.461+2914A>G	NP_001350330.1:n.461+2914A>G
XM_017008413.1:c.461+2914A>G	XP_016863902.1:n.461+2914A>G
XM_017008414.1:c.461+2914A>G	XP_016863903.1:n.461+2914A>G
XM_017008415.1:c.461+2914A>G	XP_016863904.1:n.461+2914A>G
XM_017008416.1:c.461+2914A>G	XP_016863905.1:n.461+2914A>G
XM_017008417.1:c.461+2914A>G	XP_016863906.1:n.461+2914A>G
XM_017008418.1:c.461+2914A>G	XP_016863907.1:n.461+2914A>G
NM_001282485.2:c.461+2914A>G	NP_001269414.1:n.461+2914A>G
NM_001363401.2:c.461+2914A>G	NP_001350330.1:n.461+2914A>G
NM_006259.3:c.461+2914A>G MANE Select	NP_006250.1:n.461+2914A>G