ClinVar

NM_005343.4(HRAS):c.*76G>C

Genes:

HRAS:HRas proto-oncogene, GTPase [Gene - OMIM - HGNC]
LRRC56:leucine rich repeat containing 56 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

• Chr11: 532452 (on Assembly GRCh38)
• Chr11: 532452 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.*76G>C

HGVS:

• NC_000011.10:g.532452C>G
• NG_007666.1:g.8099G>C
• NM_001130442.3:c.*184G>C
• NM_001318054.2:c.*76G>C
• NM_005343.4:c.*76G>CMANE SELECT
• NM_176795.5:c.*323G>C
• LRG_506t1:c.*76G>C
• LRG_506:g.8099G>C
• NC_000011.9:g.532452C>G

This HGVS expression did not pass validation

Links:

dbSNP: rs45565838

NCBI 1000 Genomes Browser:

rs45565838

Molecular consequence:

• NM_001130442.3:c.*184G>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001318054.2:c.*76G>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_005343.4:c.*76G>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_176795.5:c.*323G>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]