ClinVar

NM_000540.3(RYR1):c.7872C>T (p.Arg2624=)

Gene:

RYR1:ryanodine receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 38502916 (on Assembly GRCh38)
• Chr19: 38993556 (on Assembly GRCh37)

Preferred name:

NM_000540.3(RYR1):c.7872C>T (p.Arg2624=)

HGVS:

• NC_000019.10:g.38502916C>T
• NG_008866.1:g.74217C>T
• NM_000540.3:c.7872C>TMANE SELECT
• NM_001042723.2:c.7872C>T
• NP_000531.2:p.Arg2624=
• NP_000531.2:p.Arg2624=
• NP_001036188.1:p.Arg2624=
• LRG_766t1:c.7872C>T
• LRG_766:g.74217C>T
• LRG_766p1:p.Arg2624=
• NC_000019.9:g.38993556C>T
• NM_000540.2:c.7872C>T
• NP_000531.2:p.(=)
• p.Arg2624Arg

This HGVS expression did not pass validation

Links:

dbSNP: rs1469698

NCBI 1000 Genomes Browser:

rs1469698

Molecular consequence:

• NM_000540.3:c.7872C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001042723.2:c.7872C>T - synonymous variant - [Sequence Ontology: SO:0001819]