Canonical Allele Identifier: CA733323803

Gene: RYR2

Linked Data

• dbSNP Id: rs1345104955
• gnomAD v3: 1-237770729-T-C
• gnomAD v4: 1-237770729-T-C
• MyVariant Identifiers: chr1:g.237934029T>C (hg19) ; chr1:g.237770729T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237770729T>C , CM000663.2:g.237770729T>C	GRCh38
NC_000001.10:g.237934029T>C , CM000663.1:g.237934029T>C	GRCh37
NC_000001.9:g.236000652T>C	NCBI36
NG_008799.2:g.733328T>C
NG_008799.3:g.733546T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*2569-78T>C	ENSP00000499659.2:n.*2569-78T>C
ENST00000659194.3:c.11465-78T>C	ENSP00000499653.3:n.11465-78T>C
ENST00000660292.2:c.11498-78T>C	ENSP00000499787.2:n.11498-78T>C
ENST00000659194.2:c.3654-78T>C
ENST00000366574.7:c.11477-78T>C MANE Select	ENSP00000355533.2:n.11477-78T>C
ENST00000659194.1:c.3654-78T>C
ENST00000660292.1:c.1530-78T>C
ENST00000360064.7:c.11429-78T>C	ENSP00000353174.7:n.11429-78T>C
ENST00000366574.6:c.11477-78T>C	ENSP00000355533.2:n.11477-78T>C
ENST00000609119.1:n.2672-78T>C
NM_001035.2:c.11477-78T>C	NP_001026.2:n.11477-78T>C
XM_006711802.2:c.11531-78T>C	XP_006711865.1:n.11531-78T>C
XM_006711803.2:c.11528-78T>C	XP_006711866.1:n.11528-78T>C
XM_006711804.2:c.11507-78T>C	XP_006711867.1:n.11507-78T>C
XM_006711805.2:c.11501-78T>C	XP_006711868.1:n.11501-78T>C
XM_006711806.2:c.11495-78T>C	XP_006711869.1:n.11495-78T>C
XM_006711807.2:c.11471-78T>C	XP_006711870.1:n.11471-78T>C
XM_006711808.2:c.11294-78T>C	XP_006711871.1:n.11294-78T>C
XM_006711810.2:c.11438-78T>C	XP_006711873.1:n.11438-78T>C
XM_006711802.3:c.11531-78T>C	XP_006711865.1:n.11531-78T>C
XM_006711803.3:c.11528-78T>C	XP_006711866.1:n.11528-78T>C
XM_006711804.3:c.11507-78T>C	XP_006711867.1:n.11507-78T>C
XM_006711805.3:c.11501-78T>C	XP_006711868.1:n.11501-78T>C
XM_006711806.3:c.11495-78T>C	XP_006711869.1:n.11495-78T>C
XM_006711807.3:c.11471-78T>C	XP_006711870.1:n.11471-78T>C
XM_006711808.3:c.11294-78T>C	XP_006711871.1:n.11294-78T>C
XM_006711810.3:c.11438-78T>C	XP_006711873.1:n.11438-78T>C
XM_017002028.1:c.11510-78T>C	XP_016857517.1:n.11510-78T>C
NM_001035.3:c.11477-78T>C MANE Select	NP_001026.2:n.11477-78T>C