Canonical Allele Identifier: CA345411014

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237791223A>T (hg19) ; chr1:g.237627923A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237627923A>T , CM000663.2:g.237627923A>T	GRCh38
NC_000001.10:g.237791223A>T , CM000663.1:g.237791223A>T	GRCh37
NC_000001.9:g.235857846A>T	NCBI36
NG_008799.2:g.590522A>T
NG_008799.3:g.590740A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6283A>T	ENSP00000499659.2:p.Ile2095Phe
ENST00000659194.3:c.6283A>T	ENSP00000499653.3:p.Ile2095Phe
ENST00000660292.2:c.6283A>T	ENSP00000499787.2:p.Ile2095Phe
ENST00000366574.7:c.6283A>T MANE Select	ENSP00000355533.2:p.Ile2095Phe
ENST00000360064.7:c.6235A>T	ENSP00000353174.7:p.Ile2079Phe
ENST00000366574.6:c.6283A>T	ENSP00000355533.2:p.Ile2095Phe
NM_001035.2:c.6283A>T	NP_001026.2:p.Ile2095Phe
XM_006711802.2:c.6313A>T	XP_006711865.1:p.Ile2105Phe
XM_006711803.2:c.6310A>T	XP_006711866.1:p.Ile2104Phe
XM_006711804.2:c.6313A>T	XP_006711867.1:p.Ile2105Phe
XM_006711805.2:c.6283A>T	XP_006711868.1:p.Ile2095Phe
XM_006711806.2:c.6313A>T	XP_006711869.1:p.Ile2105Phe
XM_006711807.2:c.6313A>T	XP_006711870.1:p.Ile2105Phe
XM_006711808.2:c.6313A>T	XP_006711871.1:p.Ile2105Phe
XM_006711809.2:c.6313A>T	XP_006711872.1:p.Ile2105Phe
XM_006711810.2:c.6280A>T	XP_006711873.1:p.Ile2094Phe
XR_949152.1:n.6594A>T
XM_006711802.3:c.6313A>T	XP_006711865.1:p.Ile2105Phe
XM_006711803.3:c.6310A>T	XP_006711866.1:p.Ile2104Phe
XM_006711804.3:c.6313A>T	XP_006711867.1:p.Ile2105Phe
XM_006711805.3:c.6283A>T	XP_006711868.1:p.Ile2095Phe
XM_006711806.3:c.6313A>T	XP_006711869.1:p.Ile2105Phe
XM_006711807.3:c.6313A>T	XP_006711870.1:p.Ile2105Phe
XM_006711808.3:c.6313A>T	XP_006711871.1:p.Ile2105Phe
XM_006711810.3:c.6280A>T	XP_006711873.1:p.Ile2094Phe
XM_017002028.1:c.6292A>T	XP_016857517.1:p.Ile2098Phe
XR_002957299.1:n.6627A>T
XR_949152.2:n.6627A>T
NM_001035.3:c.6283A>T MANE Select	NP_001026.2:p.Ile2095Phe