Canonical Allele Identifier: CA405679435
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070935
ClinVar RCV Id: RCV004014437
dbSNP Id: rs1568438505
MyVariant Identifiers: chr19:g.38937141C>T (hg19) chr19:g.38446501C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38446501C>T , CM000681.2:g.38446501C>T GRCh38
NC_000019.9:g.38937141C>T , CM000681.1:g.38937141C>T GRCh37
NC_000019.8:g.43628981C>T NCBI36
NG_008866.1:g.17802C>T , LRG_766:g.17802C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.661C>T ENSP00000471601.2:p.Leu221Phe
ENST00000359596.8:c.661C>T MANE Select ENSP00000352608.2:p.Leu221Phe
ENST00000355481.8:c.661C>T ENSP00000347667.3:p.Leu221Phe
ENST00000359596.7:c.661C>T ENSP00000352608.2:p.Leu221Phe
ENST00000360985.7:c.661C>T ENSP00000354254.4:p.Leu221Phe
NM_000540.2:c.661C>T , LRG_766t1:c.661C>T NP_000531.2:p.Leu221Phe
NM_001042723.1:c.661C>T NP_001036188.1:p.Leu221Phe
XM_006723317.1:c.661C>T XP_006723380.1:p.Leu221Phe
XM_006723319.1:c.661C>T XP_006723382.1:p.Leu221Phe
XM_011527204.1:c.661C>T XP_011525506.1:p.Leu221Phe
XM_011527205.1:c.661C>T XP_011525507.1:p.Leu221Phe
XM_006723317.2:c.661C>T XP_006723380.1:p.Leu221Phe
XM_006723319.2:c.661C>T XP_006723382.1:p.Leu221Phe
XM_011527205.2:c.661C>T XP_011525507.1:p.Leu221Phe
XR_001753735.1:n.744C>T
NM_000540.3:c.661C>T MANE Select NP_000531.2:p.Leu221Phe
NM_001042723.2:c.661C>T NP_001036188.1:p.Leu221Phe
Search 100 bp 5'
Search 100 bp 3'