Canonical Allele Identifier: CA345383698

Gene: RYR2

Linked Data

• ClinVar Variation Id: 618352
• ClinVar RCV Id: RCV000756608 ; RCV001179696 ; RCV002533793 ; RCV003999887
• dbSNP Id: rs377368967
• gnomAD v4: 1-237417090-G-A
• COSMIC: COSM4029882 ; COSM4029883
• MyVariant Identifiers: chr1:g.237580390G>A (hg19) ; chr1:g.237417090G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.815G>A	ENSP00000499659.2:p.Arg272His
ENST00000659194.3:c.815G>A	ENSP00000499653.3:p.Arg272His
ENST00000660292.2:c.815G>A	ENSP00000499787.2:p.Arg272His
ENST00000366574.7:c.815G>A MANE Select	ENSP00000355533.2:p.Arg272His
ENST00000360064.7:c.767G>A	ENSP00000353174.7:p.Arg256His
ENST00000366574.6:c.815G>A	ENSP00000355533.2:p.Arg272His
NM_001035.2:c.815G>A	NP_001026.2:p.Arg272His
XM_006711802.2:c.815G>A	XP_006711865.1:p.Arg272His
XM_006711803.2:c.815G>A	XP_006711866.1:p.Arg272His
XM_006711804.2:c.815G>A	XP_006711867.1:p.Arg272His
XM_006711805.2:c.815G>A	XP_006711868.1:p.Arg272His
XM_006711806.2:c.815G>A	XP_006711869.1:p.Arg272His
XM_006711807.2:c.815G>A	XP_006711870.1:p.Arg272His
XM_006711808.2:c.815G>A	XP_006711871.1:p.Arg272His
XM_006711809.2:c.815G>A	XP_006711872.1:p.Arg272His
XM_006711810.2:c.815G>A	XP_006711873.1:p.Arg272His
XR_949152.1:n.1096G>A
XM_006711802.3:c.815G>A	XP_006711865.1:p.Arg272His
XM_006711803.3:c.815G>A	XP_006711866.1:p.Arg272His
XM_006711804.3:c.815G>A	XP_006711867.1:p.Arg272His
XM_006711805.3:c.815G>A	XP_006711868.1:p.Arg272His
XM_006711806.3:c.815G>A	XP_006711869.1:p.Arg272His
XM_006711807.3:c.815G>A	XP_006711870.1:p.Arg272His
XM_006711808.3:c.815G>A	XP_006711871.1:p.Arg272His
XM_006711810.3:c.815G>A	XP_006711873.1:p.Arg272His
XM_017002028.1:c.794G>A	XP_016857517.1:p.Arg265His
XR_002957299.1:n.1129G>A
XR_949152.2:n.1129G>A
NM_001035.3:c.815G>A MANE Select	NP_001026.2:p.Arg272His