Canonical Allele Identifier: CA423819704

Gene: RYR2

Linked Data

• dbSNP Id: rs1682398018
• MyVariant Identifiers: chr1:g.237811799A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237648499A>G , CM000663.2:g.237648499A>G	GRCh38
NC_000001.10:g.237811799A>G , CM000663.1:g.237811799A>G	GRCh37
NC_000001.9:g.235878422A>G	NCBI36
NG_008799.2:g.611098A>G
NG_008799.3:g.611316A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000609119.2:c.7398A>G	ENSP00000499659.2:p.Ala2466=
ENST00000659194.3:c.7398A>G	ENSP00000499653.3:p.Ala2466=
ENST00000660292.2:c.7398A>G	ENSP00000499787.2:p.Ala2466=
ENST00000366574.7:c.7398A>G MANE Select	ENSP00000355533.2:p.Ala2466=
ENST00000360064.7:c.7350A>G	ENSP00000353174.7:p.Ala2450=
ENST00000366574.6:c.7398A>G	ENSP00000355533.2:p.Ala2466=
NM_001035.2:c.7398A>G	NP_001026.2:p.Ala2466=
XM_006711802.2:c.7428A>G	XP_006711865.1:p.Ala2476=
XM_006711803.2:c.7425A>G	XP_006711866.1:p.Ala2475=
XM_006711804.2:c.7428A>G	XP_006711867.1:p.Ala2476=
XM_006711805.2:c.7398A>G	XP_006711868.1:p.Ala2466=
XM_006711806.2:c.7428A>G	XP_006711869.1:p.Ala2476=
XM_006711807.2:c.7428A>G	XP_006711870.1:p.Ala2476=
XM_006711808.2:c.7428A>G	XP_006711871.1:p.Ala2476=
XM_006711809.2:c.7428A>G	XP_006711872.1:p.Ala2476=
XM_006711810.2:c.7395A>G	XP_006711873.1:p.Ala2465=
XR_949152.1:n.7709A>G
XM_006711802.3:c.7428A>G	XP_006711865.1:p.Ala2476=
XM_006711803.3:c.7425A>G	XP_006711866.1:p.Ala2475=
XM_006711804.3:c.7428A>G	XP_006711867.1:p.Ala2476=
XM_006711805.3:c.7398A>G	XP_006711868.1:p.Ala2466=
XM_006711806.3:c.7428A>G	XP_006711869.1:p.Ala2476=
XM_006711807.3:c.7428A>G	XP_006711870.1:p.Ala2476=
XM_006711808.3:c.7428A>G	XP_006711871.1:p.Ala2476=
XM_006711810.3:c.7395A>G	XP_006711873.1:p.Ala2465=
XM_017002028.1:c.7407A>G	XP_016857517.1:p.Ala2469=
XR_002957299.1:n.7742A>G
XR_949152.2:n.7742A>G
NM_001035.3:c.7398A>G MANE Select	NP_001026.2:p.Ala2466=