Canonical Allele Identifier: CA39774103

Gene: RYR2

Linked Data

• dbSNP Id: rs948507238
• gnomAD v3: 1-237377271-G-T
• gnomAD v4: 1-237377271-G-T
• MyVariant Identifiers: chr1:g.237540571G>T (hg19) ; chr1:g.237377271G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237377271G>T , CM000663.2:g.237377271G>T	GRCh38
NC_000001.10:g.237540571G>T , CM000663.1:g.237540571G>T	GRCh37
NC_000001.9:g.235607194G>T	NCBI36
NG_008799.2:g.339870G>T
NG_008799.3:g.340088G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609119.2:c.464-52G>T	ENSP00000499659.2:n.464-52G>T
ENST00000659194.3:c.464-52G>T	ENSP00000499653.3:n.464-52G>T
ENST00000660292.2:c.464-52G>T	ENSP00000499787.2:n.464-52G>T
ENST00000366574.7:c.464-52G>T MANE Select	ENSP00000355533.2:n.464-52G>T
ENST00000360064.7:c.416-52G>T	ENSP00000353174.7:n.416-52G>T
ENST00000366574.6:c.464-52G>T	ENSP00000355533.2:n.464-52G>T
NM_001035.2:c.464-52G>T	NP_001026.2:n.464-52G>T
XM_006711802.2:c.464-52G>T	XP_006711865.1:n.464-52G>T
XM_006711803.2:c.464-52G>T	XP_006711866.1:n.464-52G>T
XM_006711804.2:c.464-52G>T	XP_006711867.1:n.464-52G>T
XM_006711805.2:c.464-52G>T	XP_006711868.1:n.464-52G>T
XM_006711806.2:c.464-52G>T	XP_006711869.1:n.464-52G>T
XM_006711807.2:c.464-52G>T	XP_006711870.1:n.464-52G>T
XM_006711808.2:c.464-52G>T	XP_006711871.1:n.464-52G>T
XM_006711809.2:c.464-52G>T	XP_006711872.1:n.464-52G>T
XM_006711810.2:c.464-52G>T	XP_006711873.1:n.464-52G>T
XR_949152.1:n.745-52G>T
XM_006711802.3:c.464-52G>T	XP_006711865.1:n.464-52G>T
XM_006711803.3:c.464-52G>T	XP_006711866.1:n.464-52G>T
XM_006711804.3:c.464-52G>T	XP_006711867.1:n.464-52G>T
XM_006711805.3:c.464-52G>T	XP_006711868.1:n.464-52G>T
XM_006711806.3:c.464-52G>T	XP_006711869.1:n.464-52G>T
XM_006711807.3:c.464-52G>T	XP_006711870.1:n.464-52G>T
XM_006711808.3:c.464-52G>T	XP_006711871.1:n.464-52G>T
XM_006711810.3:c.464-52G>T	XP_006711873.1:n.464-52G>T
XM_017002028.1:c.443-52G>T	XP_016857517.1:n.443-52G>T
XR_002957299.1:n.778-52G>T
XR_949152.2:n.778-52G>T
NM_001035.3:c.464-52G>T MANE Select	NP_001026.2:n.464-52G>T