Canonical Allele Identifier: CA345411212

Gene: RYR2

Linked Data

• ClinVar Variation Id: 2774320
• ClinVar RCV Id: RCV003533400
• gnomAD v4: 1-237627953-A-G
• MyVariant Identifiers: chr1:g.237791253A>G (hg19) ; chr1:g.237627953A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237627953A>G , CM000663.2:g.237627953A>G	GRCh38
NC_000001.10:g.237791253A>G , CM000663.1:g.237791253A>G	GRCh37
NC_000001.9:g.235857876A>G	NCBI36
NG_008799.2:g.590552A>G
NG_008799.3:g.590770A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6313A>G	ENSP00000499659.2:p.Thr2105Ala
ENST00000659194.3:c.6313A>G	ENSP00000499653.3:p.Thr2105Ala
ENST00000660292.2:c.6313A>G	ENSP00000499787.2:p.Thr2105Ala
ENST00000366574.7:c.6313A>G MANE Select	ENSP00000355533.2:p.Thr2105Ala
ENST00000360064.7:c.6265A>G	ENSP00000353174.7:p.Thr2089Ala
ENST00000366574.6:c.6313A>G	ENSP00000355533.2:p.Thr2105Ala
NM_001035.2:c.6313A>G	NP_001026.2:p.Thr2105Ala
XM_006711802.2:c.6343A>G	XP_006711865.1:p.Thr2115Ala
XM_006711803.2:c.6340A>G	XP_006711866.1:p.Thr2114Ala
XM_006711804.2:c.6343A>G	XP_006711867.1:p.Thr2115Ala
XM_006711805.2:c.6313A>G	XP_006711868.1:p.Thr2105Ala
XM_006711806.2:c.6343A>G	XP_006711869.1:p.Thr2115Ala
XM_006711807.2:c.6343A>G	XP_006711870.1:p.Thr2115Ala
XM_006711808.2:c.6343A>G	XP_006711871.1:p.Thr2115Ala
XM_006711809.2:c.6343A>G	XP_006711872.1:p.Thr2115Ala
XM_006711810.2:c.6310A>G	XP_006711873.1:p.Thr2104Ala
XR_949152.1:n.6624A>G
XM_006711802.3:c.6343A>G	XP_006711865.1:p.Thr2115Ala
XM_006711803.3:c.6340A>G	XP_006711866.1:p.Thr2114Ala
XM_006711804.3:c.6343A>G	XP_006711867.1:p.Thr2115Ala
XM_006711805.3:c.6313A>G	XP_006711868.1:p.Thr2105Ala
XM_006711806.3:c.6343A>G	XP_006711869.1:p.Thr2115Ala
XM_006711807.3:c.6343A>G	XP_006711870.1:p.Thr2115Ala
XM_006711808.3:c.6343A>G	XP_006711871.1:p.Thr2115Ala
XM_006711810.3:c.6310A>G	XP_006711873.1:p.Thr2104Ala
XM_017002028.1:c.6322A>G	XP_016857517.1:p.Thr2108Ala
XR_002957299.1:n.6657A>G
XR_949152.2:n.6657A>G
NM_001035.3:c.6313A>G MANE Select	NP_001026.2:p.Thr2105Ala