Canonical Allele Identifier: CA345413878

Gene: RYR2

Linked Data

• dbSNP Id: rs147887477
• MyVariant Identifiers: chr1:g.237947681G>T (hg19) ; chr1:g.237784381G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784381G>T , CM000663.2:g.237784381G>T	GRCh38
NC_000001.10:g.237947681G>T , CM000663.1:g.237947681G>T	GRCh37
NC_000001.9:g.236014304G>T	NCBI36
NG_008799.2:g.746980G>T
NG_008799.3:g.747198G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3761G>T	ENSP00000499659.2:n.*3761G>T
ENST00000659194.3:c.12657G>T	ENSP00000499653.3:p.Lys4219Asn
ENST00000660292.2:c.12690G>T	ENSP00000499787.2:p.Lys4230Asn
ENST00000659194.2:c.4846G>T
ENST00000366574.7:c.12669G>T MANE Select	ENSP00000355533.2:p.Lys4223Asn
ENST00000659194.1:c.4846G>T
ENST00000660292.1:c.2722G>T
ENST00000360064.7:c.12621G>T	ENSP00000353174.7:p.Lys4207Asn
ENST00000366574.6:c.12669G>T	ENSP00000355533.2:p.Lys4223Asn
ENST00000609119.1:n.3864G>T
NM_001035.2:c.12669G>T	NP_001026.2:p.Lys4223Asn
XM_006711802.2:c.12723G>T	XP_006711865.1:p.Lys4241Asn
XM_006711803.2:c.12720G>T	XP_006711866.1:p.Lys4240Asn
XM_006711804.2:c.12699G>T	XP_006711867.1:p.Lys4233Asn
XM_006711805.2:c.12693G>T	XP_006711868.1:p.Lys4231Asn
XM_006711806.2:c.12687G>T	XP_006711869.1:p.Lys4229Asn
XM_006711807.2:c.12663G>T	XP_006711870.1:p.Lys4221Asn
XM_006711808.2:c.12486G>T	XP_006711871.1:p.Lys4162Asn
XM_006711810.2:c.12630G>T	XP_006711873.1:p.Lys4210Asn
XM_006711802.3:c.12723G>T	XP_006711865.1:p.Lys4241Asn
XM_006711803.3:c.12720G>T	XP_006711866.1:p.Lys4240Asn
XM_006711804.3:c.12699G>T	XP_006711867.1:p.Lys4233Asn
XM_006711805.3:c.12693G>T	XP_006711868.1:p.Lys4231Asn
XM_006711806.3:c.12687G>T	XP_006711869.1:p.Lys4229Asn
XM_006711807.3:c.12663G>T	XP_006711870.1:p.Lys4221Asn
XM_006711808.3:c.12486G>T	XP_006711871.1:p.Lys4162Asn
XM_006711810.3:c.12630G>T	XP_006711873.1:p.Lys4210Asn
XM_017002028.1:c.12702G>T	XP_016857517.1:p.Lys4234Asn
NM_001035.3:c.12669G>T MANE Select	NP_001026.2:p.Lys4223Asn