ClinVar

NM_003839.4(TNFRSF11A):c.-39G>A

Genes:

LOC130062628:ATAC-STARR-seq lymphoblastoid silent region 9505 [Gene]
TNFRSF11A:TNF receptor superfamily member 11a [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

18q21.33

Genomic location:

• Chr18: 62325314 (on Assembly GRCh38)
• Chr18: 59992547 (on Assembly GRCh37)

Preferred name:

NM_003839.4(TNFRSF11A):c.-39G>A

HGVS:

• NC_000018.10:g.62325314G>A
• NG_008098.1:g.5000G>A
• NM_001270949.2:c.-39G>A
• NM_001270950.2:c.-39G>A
• NM_001270951.2:c.-39G>A
• NM_001278268.2:c.-39G>A
• NM_003839.4:c.-39G>AMANE SELECT
• LRG_194:g.5000G>A
• NC_000018.9:g.59992547G>A
• NM_003839.3:c.-39G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs7238731

NCBI 1000 Genomes Browser:

rs7238731

Molecular consequence:

• NM_001270949.2:c.-39G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001270950.2:c.-39G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001270951.2:c.-39G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001278268.2:c.-39G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_003839.4:c.-39G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]