Canonical Allele Identifier: CA345413516

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947525G>T (hg19) ; chr1:g.237784225G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784225G>T , CM000663.2:g.237784225G>T	GRCh38
NC_000001.10:g.237947525G>T , CM000663.1:g.237947525G>T	GRCh37
NC_000001.9:g.236014148G>T	NCBI36
NG_008799.2:g.746824G>T
NG_008799.3:g.747042G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609119.2:c.*3605G>T	ENSP00000499659.2:n.*3605G>T
ENST00000659194.3:c.12501G>T	ENSP00000499653.3:p.Gln4167His
ENST00000660292.2:c.12534G>T	ENSP00000499787.2:p.Gln4178His
ENST00000659194.2:c.4690G>T
ENST00000366574.7:c.12513G>T MANE Select	ENSP00000355533.2:p.Gln4171His
ENST00000659194.1:c.4690G>T
ENST00000660292.1:c.2566G>T
ENST00000360064.7:c.12465G>T	ENSP00000353174.7:p.Gln4155His
ENST00000366574.6:c.12513G>T	ENSP00000355533.2:p.Gln4171His
ENST00000609119.1:n.3708G>T
NM_001035.2:c.12513G>T	NP_001026.2:p.Gln4171His
XM_006711802.2:c.12567G>T	XP_006711865.1:p.Gln4189His
XM_006711803.2:c.12564G>T	XP_006711866.1:p.Gln4188His
XM_006711804.2:c.12543G>T	XP_006711867.1:p.Gln4181His
XM_006711805.2:c.12537G>T	XP_006711868.1:p.Gln4179His
XM_006711806.2:c.12531G>T	XP_006711869.1:p.Gln4177His
XM_006711807.2:c.12507G>T	XP_006711870.1:p.Gln4169His
XM_006711808.2:c.12330G>T	XP_006711871.1:p.Gln4110His
XM_006711810.2:c.12474G>T	XP_006711873.1:p.Gln4158His
XM_006711802.3:c.12567G>T	XP_006711865.1:p.Gln4189His
XM_006711803.3:c.12564G>T	XP_006711866.1:p.Gln4188His
XM_006711804.3:c.12543G>T	XP_006711867.1:p.Gln4181His
XM_006711805.3:c.12537G>T	XP_006711868.1:p.Gln4179His
XM_006711806.3:c.12531G>T	XP_006711869.1:p.Gln4177His
XM_006711807.3:c.12507G>T	XP_006711870.1:p.Gln4169His
XM_006711808.3:c.12330G>T	XP_006711871.1:p.Gln4110His
XM_006711810.3:c.12474G>T	XP_006711873.1:p.Gln4158His
XM_017002028.1:c.12546G>T	XP_016857517.1:p.Gln4182His
NM_001035.3:c.12513G>T MANE Select	NP_001026.2:p.Gln4171His