Canonical Allele Identifier: CA345396621

Gene: RYR2

Linked Data

• ClinVar Variation Id: 1332566
• ClinVar RCV Id: RCV001805612
• dbSNP Id: rs2148738458
• MyVariant Identifiers: chr1:g.237804228C>T (hg19) ; chr1:g.237640928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237640928C>T , CM000663.2:g.237640928C>T	GRCh38
NC_000001.10:g.237804228C>T , CM000663.1:g.237804228C>T	GRCh37
NC_000001.9:g.235870851C>T	NCBI36
NG_008799.2:g.603527C>T
NG_008799.3:g.603745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.7147C>T	ENSP00000499659.2:p.His2383Tyr
ENST00000659194.3:c.7147C>T	ENSP00000499653.3:p.His2383Tyr
ENST00000660292.2:c.7147C>T	ENSP00000499787.2:p.His2383Tyr
ENST00000366574.7:c.7147C>T MANE Select	ENSP00000355533.2:p.His2383Tyr
ENST00000360064.7:c.7099C>T	ENSP00000353174.7:p.His2367Tyr
ENST00000366574.6:c.7147C>T	ENSP00000355533.2:p.His2383Tyr
NM_001035.2:c.7147C>T	NP_001026.2:p.His2383Tyr
XM_006711802.2:c.7177C>T	XP_006711865.1:p.His2393Tyr
XM_006711803.2:c.7174C>T	XP_006711866.1:p.His2392Tyr
XM_006711804.2:c.7177C>T	XP_006711867.1:p.His2393Tyr
XM_006711805.2:c.7147C>T	XP_006711868.1:p.His2383Tyr
XM_006711806.2:c.7177C>T	XP_006711869.1:p.His2393Tyr
XM_006711807.2:c.7177C>T	XP_006711870.1:p.His2393Tyr
XM_006711808.2:c.7177C>T	XP_006711871.1:p.His2393Tyr
XM_006711809.2:c.7177C>T	XP_006711872.1:p.His2393Tyr
XM_006711810.2:c.7144C>T	XP_006711873.1:p.His2382Tyr
XR_949152.1:n.7458C>T
XM_006711802.3:c.7177C>T	XP_006711865.1:p.His2393Tyr
XM_006711803.3:c.7174C>T	XP_006711866.1:p.His2392Tyr
XM_006711804.3:c.7177C>T	XP_006711867.1:p.His2393Tyr
XM_006711805.3:c.7147C>T	XP_006711868.1:p.His2383Tyr
XM_006711806.3:c.7177C>T	XP_006711869.1:p.His2393Tyr
XM_006711807.3:c.7177C>T	XP_006711870.1:p.His2393Tyr
XM_006711808.3:c.7177C>T	XP_006711871.1:p.His2393Tyr
XM_006711810.3:c.7144C>T	XP_006711873.1:p.His2382Tyr
XM_017002028.1:c.7156C>T	XP_016857517.1:p.His2386Tyr
XR_002957299.1:n.7491C>T
XR_949152.2:n.7491C>T
NM_001035.3:c.7147C>T MANE Select	NP_001026.2:p.His2383Tyr