Canonical Allele Identifier: CA632876635
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1226968208
gnomAD v2: 19-39068734-G-T
gnomAD v4: 19-38578094-G-T
MyVariant Identifiers: chr19:g.39068734G>T (hg19) chr19:g.38578094G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578094G>T , CM000681.2:g.38578094G>T GRCh38
NC_000019.9:g.39068734G>T , CM000681.1:g.39068734G>T GRCh37
NC_000019.8:g.43760574G>T NCBI36
NG_008866.1:g.149395G>T , LRG_766:g.149395G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1239+46G>T
ENST00000688602.1:c.2636+46G>T
ENST00000689936.1:c.2608+46G>T
ENST00000359596.8:c.14303+46G>T MANE Select ENSP00000352608.2:n.14303+46G>T
ENST00000355481.8:c.14288+46G>T ENSP00000347667.3:n.14288+46G>T
ENST00000359596.7:c.14303+46G>T ENSP00000352608.2:n.14303+46G>T
ENST00000360985.7:c.14285+46G>T ENSP00000354254.4:n.14285+46G>T
NM_000540.2:c.14303+46G>T , LRG_766t1:c.14303+46G>T NP_000531.2:n.14303+46G>T
NM_001042723.1:c.14288+46G>T NP_001036188.1:n.14288+46G>T
XM_006723317.1:c.14285+46G>T XP_006723380.1:n.14285+46G>T
XM_006723319.1:c.14270+46G>T XP_006723382.1:n.14270+46G>T
XM_011527204.1:c.14300+46G>T XP_011525506.1:n.14300+46G>T
XM_011527205.1:c.14216+46G>T XP_011525507.1:n.14216+46G>T
XM_006723317.2:c.14285+46G>T XP_006723380.1:n.14285+46G>T
XM_006723319.2:c.14270+46G>T XP_006723382.1:n.14270+46G>T
XM_011527205.2:c.14216+46G>T XP_011525507.1:n.14216+46G>T
NM_000540.3:c.14303+46G>T MANE Select NP_000531.2:n.14303+46G>T
NM_001042723.2:c.14288+46G>T NP_001036188.1:n.14288+46G>T
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