Canonical Allele Identifier: CA423808698

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237540645A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237377345A>C , CM000663.2:g.237377345A>C	GRCh38
NC_000001.10:g.237540645A>C , CM000663.1:g.237540645A>C	GRCh37
NC_000001.9:g.235607268A>C	NCBI36
NG_008799.2:g.339944A>C
NG_008799.3:g.340162A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.486A>C	ENSP00000499659.2:p.Ile162=
ENST00000659194.3:c.486A>C	ENSP00000499653.3:p.Ile162=
ENST00000660292.2:c.486A>C	ENSP00000499787.2:p.Ile162=
ENST00000366574.7:c.486A>C MANE Select	ENSP00000355533.2:p.Ile162=
ENST00000360064.7:c.438A>C	ENSP00000353174.7:p.Ile146=
ENST00000366574.6:c.486A>C	ENSP00000355533.2:p.Ile162=
NM_001035.2:c.486A>C	NP_001026.2:p.Ile162=
XM_006711802.2:c.486A>C	XP_006711865.1:p.Ile162=
XM_006711803.2:c.486A>C	XP_006711866.1:p.Ile162=
XM_006711804.2:c.486A>C	XP_006711867.1:p.Ile162=
XM_006711805.2:c.486A>C	XP_006711868.1:p.Ile162=
XM_006711806.2:c.486A>C	XP_006711869.1:p.Ile162=
XM_006711807.2:c.486A>C	XP_006711870.1:p.Ile162=
XM_006711808.2:c.486A>C	XP_006711871.1:p.Ile162=
XM_006711809.2:c.486A>C	XP_006711872.1:p.Ile162=
XM_006711810.2:c.486A>C	XP_006711873.1:p.Ile162=
XR_949152.1:n.767A>C
XM_006711802.3:c.486A>C	XP_006711865.1:p.Ile162=
XM_006711803.3:c.486A>C	XP_006711866.1:p.Ile162=
XM_006711804.3:c.486A>C	XP_006711867.1:p.Ile162=
XM_006711805.3:c.486A>C	XP_006711868.1:p.Ile162=
XM_006711806.3:c.486A>C	XP_006711869.1:p.Ile162=
XM_006711807.3:c.486A>C	XP_006711870.1:p.Ile162=
XM_006711808.3:c.486A>C	XP_006711871.1:p.Ile162=
XM_006711810.3:c.486A>C	XP_006711873.1:p.Ile162=
XM_017002028.1:c.465A>C	XP_016857517.1:p.Ile155=
XR_002957299.1:n.800A>C
XR_949152.2:n.800A>C
NM_001035.3:c.486A>C MANE Select	NP_001026.2:p.Ile162=