Canonical Allele Identifier: CA2487477536
Gene: RYR2 HGNC NCBI

Linked Data

dbSNP Id: rs1694302838

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237771925A>G , CM000663.2:g.237771925A>G GRCh38
NC_000001.10:g.237935225A>G , CM000663.1:g.237935225A>G GRCh37
NC_000001.9:g.236001848A>G NCBI36
NG_008799.2:g.734524A>G
NG_008799.3:g.734742A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*2650-87A>G ENSP00000499659.2:n.*2650-87A>G
ENST00000659194.3:c.11546-87A>G ENSP00000499653.3:n.11546-87A>G
ENST00000660292.2:c.11579-87A>G ENSP00000499787.2:n.11579-87A>G
ENST00000659194.2:c.3735-87A>G
ENST00000366574.7:c.11558-87A>G MANE Select ENSP00000355533.2:n.11558-87A>G
ENST00000659194.1:c.3735-87A>G
ENST00000660292.1:c.1611-87A>G
ENST00000360064.7:c.11510-87A>G ENSP00000353174.7:n.11510-87A>G
ENST00000366574.6:c.11558-87A>G ENSP00000355533.2:n.11558-87A>G
ENST00000609119.1:n.2753-87A>G
NM_001035.2:c.11558-87A>G NP_001026.2:n.11558-87A>G
XM_006711802.2:c.11612-87A>G XP_006711865.1:n.11612-87A>G
XM_006711803.2:c.11609-87A>G XP_006711866.1:n.11609-87A>G
XM_006711804.2:c.11588-87A>G XP_006711867.1:n.11588-87A>G
XM_006711805.2:c.11582-87A>G XP_006711868.1:n.11582-87A>G
XM_006711806.2:c.11576-87A>G XP_006711869.1:n.11576-87A>G
XM_006711807.2:c.11552-87A>G XP_006711870.1:n.11552-87A>G
XM_006711808.2:c.11375-87A>G XP_006711871.1:n.11375-87A>G
XM_006711810.2:c.11519-87A>G XP_006711873.1:n.11519-87A>G
XM_006711802.3:c.11612-87A>G XP_006711865.1:n.11612-87A>G
XM_006711803.3:c.11609-87A>G XP_006711866.1:n.11609-87A>G
XM_006711804.3:c.11588-87A>G XP_006711867.1:n.11588-87A>G
XM_006711805.3:c.11582-87A>G XP_006711868.1:n.11582-87A>G
XM_006711806.3:c.11576-87A>G XP_006711869.1:n.11576-87A>G
XM_006711807.3:c.11552-87A>G XP_006711870.1:n.11552-87A>G
XM_006711808.3:c.11375-87A>G XP_006711871.1:n.11375-87A>G
XM_006711810.3:c.11519-87A>G XP_006711873.1:n.11519-87A>G
XM_017002028.1:c.11591-87A>G XP_016857517.1:n.11591-87A>G
NM_001035.3:c.11558-87A>G MANE Select NP_001026.2:n.11558-87A>G