Canonical Allele Identifier: CA99611114

Gene: PRKG2

Linked Data

• dbSNP Id: rs983744706
• MyVariant Identifiers: chr4:g.82122823G>A (hg19) ; chr4:g.81201669G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.81201669G>A , CM000666.2:g.81201669G>A	GRCh38
NC_000004.11:g.82122823G>A , CM000666.1:g.82122823G>A	GRCh37
NC_000004.10:g.82341847G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264399.6:c.461+2918C>T MANE Select	ENSP00000264399.1:n.461+2918C>T
ENST00000264399.5:c.461+2918C>T	ENSP00000264399.1:n.461+2918C>T
ENST00000395578.3:c.461+2918C>T	ENSP00000378945.1:n.461+2918C>T
ENST00000628926.1:c.461+2918C>T	ENSP00000486129.1:n.461+2918C>T
NM_001282485.1:c.461+2918C>T	NP_001269414.1:n.461+2918C>T
NM_006259.2:c.461+2918C>T	NP_006250.1:n.461+2918C>T
XM_005263126.2:c.461+2918C>T	XP_005263183.1:n.461+2918C>T
XM_011532114.1:c.461+2918C>T	XP_011530416.1:n.461+2918C>T
XM_011532115.1:c.461+2918C>T	XP_011530417.1:n.461+2918C>T
XM_011532116.1:c.461+2918C>T	XP_011530418.1:n.461+2918C>T
NM_001363401.1:c.461+2918C>T	NP_001350330.1:n.461+2918C>T
XM_017008413.1:c.461+2918C>T	XP_016863902.1:n.461+2918C>T
XM_017008414.1:c.461+2918C>T	XP_016863903.1:n.461+2918C>T
XM_017008415.1:c.461+2918C>T	XP_016863904.1:n.461+2918C>T
XM_017008416.1:c.461+2918C>T	XP_016863905.1:n.461+2918C>T
XM_017008417.1:c.461+2918C>T	XP_016863906.1:n.461+2918C>T
XM_017008418.1:c.461+2918C>T	XP_016863907.1:n.461+2918C>T
NM_001282485.2:c.461+2918C>T	NP_001269414.1:n.461+2918C>T
NM_001363401.2:c.461+2918C>T	NP_001350330.1:n.461+2918C>T
NM_006259.3:c.461+2918C>T MANE Select	NP_006250.1:n.461+2918C>T