Canonical Allele Identifier: CA1013770180

Gene: RYR2

Linked Data

• dbSNP Id: rs1660980505
• gnomAD v3: 1-237809120-G-A
• gnomAD v4: 1-237809120-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237809120G>A , CM000663.2:g.237809120G>A	GRCh38
NC_000001.10:g.237972420G>A , CM000663.1:g.237972420G>A	GRCh37
NC_000001.9:g.236039043G>A	NCBI36
NG_008799.2:g.771719G>A
NG_008799.3:g.771937G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5525+85G>A	ENSP00000499659.2:n.*5525+85G>A
ENST00000659194.3:c.14415+85G>A	ENSP00000499653.3:n.14415+85G>A
ENST00000660292.2:c.14454+85G>A	ENSP00000499787.2:n.14454+85G>A
ENST00000659194.2:c.6604+85G>A
ENST00000366574.7:c.14433+85G>A MANE Select	ENSP00000355533.2:n.14433+85G>A
ENST00000360064.7:c.14382+85G>A	ENSP00000353174.7:n.14382+85G>A
ENST00000366574.6:c.14433+85G>A	ENSP00000355533.2:n.14433+85G>A
ENST00000608590.5:n.944+85G>A
NM_001035.2:c.14433+85G>A	NP_001026.2:n.14433+85G>A
XM_006711802.2:c.14487+85G>A	XP_006711865.1:n.14487+85G>A
XM_006711803.2:c.14484+85G>A	XP_006711866.1:n.14484+85G>A
XM_006711804.2:c.14463+85G>A	XP_006711867.1:n.14463+85G>A
XM_006711805.2:c.14457+85G>A	XP_006711868.1:n.14457+85G>A
XM_006711806.2:c.14451+85G>A	XP_006711869.1:n.14451+85G>A
XM_006711807.2:c.14427+85G>A	XP_006711870.1:n.14427+85G>A
XM_006711808.2:c.14250+85G>A	XP_006711871.1:n.14250+85G>A
XM_006711810.2:c.14394+85G>A	XP_006711873.1:n.14394+85G>A
XM_006711802.3:c.14487+85G>A	XP_006711865.1:n.14487+85G>A
XM_006711803.3:c.14484+85G>A	XP_006711866.1:n.14484+85G>A
XM_006711804.3:c.14463+85G>A	XP_006711867.1:n.14463+85G>A
XM_006711805.3:c.14457+85G>A	XP_006711868.1:n.14457+85G>A
XM_006711806.3:c.14451+85G>A	XP_006711869.1:n.14451+85G>A
XM_006711807.3:c.14427+85G>A	XP_006711870.1:n.14427+85G>A
XM_006711808.3:c.14250+85G>A	XP_006711871.1:n.14250+85G>A
XM_006711810.3:c.14394+85G>A	XP_006711873.1:n.14394+85G>A
XM_017002028.1:c.14466+85G>A	XP_016857517.1:n.14466+85G>A
NM_001035.3:c.14433+85G>A MANE Select	NP_001026.2:n.14433+85G>A