Canonical Allele Identifier: CA423810411
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2027525
ClinVar RCV Id: RCV002858670
MyVariant Identifiers: chr1:g.237580421T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237417121T>A , CM000663.2:g.237417121T>A GRCh38
NC_000001.10:g.237580421T>A , CM000663.1:g.237580421T>A GRCh37
NC_000001.9:g.235647044T>A NCBI36
NG_008799.2:g.379720T>A
NG_008799.3:g.379938T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.846T>A ENSP00000499659.2:p.Val282=
ENST00000659194.3:c.846T>A ENSP00000499653.3:p.Val282=
ENST00000660292.2:c.846T>A ENSP00000499787.2:p.Val282=
ENST00000366574.7:c.846T>A MANE Select ENSP00000355533.2:p.Val282=
ENST00000360064.7:c.798T>A ENSP00000353174.7:p.Val266=
ENST00000366574.6:c.846T>A ENSP00000355533.2:p.Val282=
NM_001035.2:c.846T>A NP_001026.2:p.Val282=
XM_006711802.2:c.846T>A XP_006711865.1:p.Val282=
XM_006711803.2:c.846T>A XP_006711866.1:p.Val282=
XM_006711804.2:c.846T>A XP_006711867.1:p.Val282=
XM_006711805.2:c.846T>A XP_006711868.1:p.Val282=
XM_006711806.2:c.846T>A XP_006711869.1:p.Val282=
XM_006711807.2:c.846T>A XP_006711870.1:p.Val282=
XM_006711808.2:c.846T>A XP_006711871.1:p.Val282=
XM_006711809.2:c.846T>A XP_006711872.1:p.Val282=
XM_006711810.2:c.846T>A XP_006711873.1:p.Val282=
XR_949152.1:n.1127T>A
XM_006711802.3:c.846T>A XP_006711865.1:p.Val282=
XM_006711803.3:c.846T>A XP_006711866.1:p.Val282=
XM_006711804.3:c.846T>A XP_006711867.1:p.Val282=
XM_006711805.3:c.846T>A XP_006711868.1:p.Val282=
XM_006711806.3:c.846T>A XP_006711869.1:p.Val282=
XM_006711807.3:c.846T>A XP_006711870.1:p.Val282=
XM_006711808.3:c.846T>A XP_006711871.1:p.Val282=
XM_006711810.3:c.846T>A XP_006711873.1:p.Val282=
XM_017002028.1:c.825T>A XP_016857517.1:p.Val275=
XR_002957299.1:n.1160T>A
XR_949152.2:n.1160T>A
NM_001035.3:c.846T>A MANE Select NP_001026.2:p.Val282=