Canonical Allele Identifier: CA345410912

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237791211C>G (hg19) ; chr1:g.237627911C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237627911C>G , CM000663.2:g.237627911C>G	GRCh38
NC_000001.10:g.237791211C>G , CM000663.1:g.237791211C>G	GRCh37
NC_000001.9:g.235857834C>G	NCBI36
NG_008799.2:g.590510C>G
NG_008799.3:g.590728C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6271C>G	ENSP00000499659.2:p.Gln2091Glu
ENST00000659194.3:c.6271C>G	ENSP00000499653.3:p.Gln2091Glu
ENST00000660292.2:c.6271C>G	ENSP00000499787.2:p.Gln2091Glu
ENST00000366574.7:c.6271C>G MANE Select	ENSP00000355533.2:p.Gln2091Glu
ENST00000360064.7:c.6223C>G	ENSP00000353174.7:p.Gln2075Glu
ENST00000366574.6:c.6271C>G	ENSP00000355533.2:p.Gln2091Glu
NM_001035.2:c.6271C>G	NP_001026.2:p.Gln2091Glu
XM_006711802.2:c.6301C>G	XP_006711865.1:p.Gln2101Glu
XM_006711803.2:c.6298C>G	XP_006711866.1:p.Gln2100Glu
XM_006711804.2:c.6301C>G	XP_006711867.1:p.Gln2101Glu
XM_006711805.2:c.6271C>G	XP_006711868.1:p.Gln2091Glu
XM_006711806.2:c.6301C>G	XP_006711869.1:p.Gln2101Glu
XM_006711807.2:c.6301C>G	XP_006711870.1:p.Gln2101Glu
XM_006711808.2:c.6301C>G	XP_006711871.1:p.Gln2101Glu
XM_006711809.2:c.6301C>G	XP_006711872.1:p.Gln2101Glu
XM_006711810.2:c.6268C>G	XP_006711873.1:p.Gln2090Glu
XR_949152.1:n.6582C>G
XM_006711802.3:c.6301C>G	XP_006711865.1:p.Gln2101Glu
XM_006711803.3:c.6298C>G	XP_006711866.1:p.Gln2100Glu
XM_006711804.3:c.6301C>G	XP_006711867.1:p.Gln2101Glu
XM_006711805.3:c.6271C>G	XP_006711868.1:p.Gln2091Glu
XM_006711806.3:c.6301C>G	XP_006711869.1:p.Gln2101Glu
XM_006711807.3:c.6301C>G	XP_006711870.1:p.Gln2101Glu
XM_006711808.3:c.6301C>G	XP_006711871.1:p.Gln2101Glu
XM_006711810.3:c.6268C>G	XP_006711873.1:p.Gln2090Glu
XM_017002028.1:c.6280C>G	XP_016857517.1:p.Gln2094Glu
XR_002957299.1:n.6615C>G
XR_949152.2:n.6615C>G
NM_001035.3:c.6271C>G MANE Select	NP_001026.2:p.Gln2091Glu