Canonical Allele Identifier: CA087031

Gene: RYR2

Linked Data

• ClinVar Variation Id: 222789
• ClinVar RCV Id: RCV001097376 ; RCV001182247 ; RCV000208243 ; RCV000621730 ; RCV001097375
• dbSNP Id: rs376389213
• ExAC: 1:237787175 G / A
• gnomAD v2: 1-237787175-G-A
• gnomAD v3: 1-237623875-G-A
• gnomAD v4: 1-237623875-G-A
• MyVariant Identifiers: chr1:g.237787175G>A (hg19) ; chr1:g.237623875G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237623875G>A , CM000663.2:g.237623875G>A	GRCh38
NC_000001.10:g.237787175G>A , CM000663.1:g.237787175G>A	GRCh37
NC_000001.9:g.235853798G>A	NCBI36
NG_008799.2:g.586474G>A
NG_008799.3:g.586692G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6022+5G>A	ENSP00000499659.2:n.6022+5G>A
ENST00000659194.3:c.6022+5G>A	ENSP00000499653.3:n.6022+5G>A
ENST00000660292.2:c.6022+5G>A	ENSP00000499787.2:n.6022+5G>A
ENST00000366574.7:c.6022+5G>A MANE Select	ENSP00000355533.2:n.6022+5G>A
ENST00000360064.7:c.5974+5G>A	ENSP00000353174.7:n.5974+5G>A
ENST00000366574.6:c.6022+5G>A	ENSP00000355533.2:n.6022+5G>A
NM_001035.2:c.6022+5G>A	NP_001026.2:n.6022+5G>A
XM_006711802.2:c.6052+5G>A	XP_006711865.1:n.6052+5G>A
XM_006711803.2:c.6049+5G>A	XP_006711866.1:n.6049+5G>A
XM_006711804.2:c.6052+5G>A	XP_006711867.1:n.6052+5G>A
XM_006711805.2:c.6022+5G>A	XP_006711868.1:n.6022+5G>A
XM_006711806.2:c.6052+5G>A	XP_006711869.1:n.6052+5G>A
XM_006711807.2:c.6052+5G>A	XP_006711870.1:n.6052+5G>A
XM_006711808.2:c.6052+5G>A	XP_006711871.1:n.6052+5G>A
XM_006711809.2:c.6052+5G>A	XP_006711872.1:n.6052+5G>A
XM_006711810.2:c.6019+5G>A	XP_006711873.1:n.6019+5G>A
XR_949152.1:n.6333+5G>A
XM_006711802.3:c.6052+5G>A	XP_006711865.1:n.6052+5G>A
XM_006711803.3:c.6049+5G>A	XP_006711866.1:n.6049+5G>A
XM_006711804.3:c.6052+5G>A	XP_006711867.1:n.6052+5G>A
XM_006711805.3:c.6022+5G>A	XP_006711868.1:n.6022+5G>A
XM_006711806.3:c.6052+5G>A	XP_006711869.1:n.6052+5G>A
XM_006711807.3:c.6052+5G>A	XP_006711870.1:n.6052+5G>A
XM_006711808.3:c.6052+5G>A	XP_006711871.1:n.6052+5G>A
XM_006711810.3:c.6019+5G>A	XP_006711873.1:n.6019+5G>A
XM_017002028.1:c.6031+5G>A	XP_016857517.1:n.6031+5G>A
XR_002957299.1:n.6366+5G>A
XR_949152.2:n.6366+5G>A
NM_001035.3:c.6022+5G>A MANE Select	NP_001026.2:n.6022+5G>A