Canonical Allele Identifier: CA207399447
Gene: PRKG1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10824310

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52268704C>T , CM000672.2:g.52268704C>T GRCh38
NC_000010.10:g.54028464C>T , CM000672.1:g.54028464C>T GRCh37
NC_000010.9:g.53698470C>T NCBI36
NG_029982.1:g.1282554C>T

Transcript Alleles

HGVS Amino-acid change
NM_001098512.2:c.1129-2646C>T VV NP_001091982.1:p.=
NM_006258.3:c.1174-2646C>T VV NP_006249.1:p.=
XM_005269972.3:c.325-2646C>T XP_005270029.1:p.=
NM_001098512.3:c.1129-2646C>T VV
NM_006258.4:c.1174-2646C>T VV
XM_017016412.1:c.889-2646C>T XP_016871901.1:p.=
XM_017016413.1:c.871-2646C>T XP_016871902.1:p.=
XM_024448078.1:c.-36-2646C>T XP_024303846.1:p.=
ENST00000373975.2:n.623-2646C>T
ENST00000373980.8:c.1174-2646C>T ENSP00000363092.4:p.=
ENST00000373985.5:c.1129-2646C>T ENSP00000363097.2:p.=
ENST00000401604.6:c.493-2646C>T ENSP00000384200.3:p.=