ClinVar

NM_002460.4(IRF4):c.492+186G>C

Gene:

IRF4:interferon regulatory factor 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p25.3

Genomic location:

• Chr6: 396121 (on Assembly GRCh38)
• Chr6: 396121 (on Assembly GRCh37)

Preferred name:

NM_002460.4(IRF4):c.492+186G>C

HGVS:

• NC_000006.12:g.396121G>C
• NG_027728.1:g.9383G>C
• NM_001195286.2:c.492+186G>C
• NM_002460.4:c.492+186G>CMANE SELECT
• NC_000006.11:g.396121G>C

This HGVS expression did not pass validation

Links:

dbSNP: rs3823305

NCBI 1000 Genomes Browser:

rs3823305

Molecular consequence:

• NM_001195286.2:c.492+186G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_002460.4:c.492+186G>C - intron variant - [Sequence Ontology: SO:0001627]