Canonical Allele Identifier: CA1144188451
Gene: RYR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237417090G= , CM000663.2:g.237417090G= GRCh38
NC_000001.10:g.237580390G= , CM000663.1:g.237580390G= GRCh37
NC_000001.9:g.235647013G= NCBI36
NG_008799.2:g.379689G=
NG_008799.3:g.379907G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.815G= ENSP00000499659.2:p.Arg272=
ENST00000659194.3:c.815G= ENSP00000499653.3:p.Arg272=
ENST00000660292.2:c.815G= ENSP00000499787.2:p.Arg272=
ENST00000366574.7:c.815G= MANE Select ENSP00000355533.2:p.Arg272=
ENST00000360064.7:c.767G= ENSP00000353174.7:p.Arg256=
ENST00000366574.6:c.815G= ENSP00000355533.2:p.Arg272=
NM_001035.2:c.815G= NP_001026.2:p.Arg272=
XM_006711802.2:c.815G= XP_006711865.1:p.Arg272=
XM_006711803.2:c.815G= XP_006711866.1:p.Arg272=
XM_006711804.2:c.815G= XP_006711867.1:p.Arg272=
XM_006711805.2:c.815G= XP_006711868.1:p.Arg272=
XM_006711806.2:c.815G= XP_006711869.1:p.Arg272=
XM_006711807.2:c.815G= XP_006711870.1:p.Arg272=
XM_006711808.2:c.815G= XP_006711871.1:p.Arg272=
XM_006711809.2:c.815G= XP_006711872.1:p.Arg272=
XM_006711810.2:c.815G= XP_006711873.1:p.Arg272=
XR_949152.1:n.1096G=
XM_006711802.3:c.815G= XP_006711865.1:p.Arg272=
XM_006711803.3:c.815G= XP_006711866.1:p.Arg272=
XM_006711804.3:c.815G= XP_006711867.1:p.Arg272=
XM_006711805.3:c.815G= XP_006711868.1:p.Arg272=
XM_006711806.3:c.815G= XP_006711869.1:p.Arg272=
XM_006711807.3:c.815G= XP_006711870.1:p.Arg272=
XM_006711808.3:c.815G= XP_006711871.1:p.Arg272=
XM_006711810.3:c.815G= XP_006711873.1:p.Arg272=
XM_017002028.1:c.794G= XP_016857517.1:p.Arg265=
XR_002957299.1:n.1129G=
XR_949152.2:n.1129G=
NM_001035.3:c.815G= MANE Select NP_001026.2:p.Arg272=