ClinVar

NM_198576.4(AGRN):c.3752-51C>T

Gene:

AGRN:agrin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.33

Genomic location:

• Chr1: 1047961 (on Assembly GRCh38)
• Chr1: 983341 (on Assembly GRCh37)

Preferred name:

NM_198576.4(AGRN):c.3752-51C>T

HGVS:

• NC_000001.11:g.1047961C>T
• NG_016346.1:g.32839C>T
• NM_001305275.2:c.3752-51C>T
• NM_001364727.2:c.3437-51C>T
• NM_198576.4:c.3752-51C>TMANE SELECT
• LRG_198:g.32839C>T
• NC_000001.10:g.983341C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs141487918

NCBI 1000 Genomes Browser:

rs141487918

Molecular consequence:

• NM_001305275.2:c.3752-51C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001364727.2:c.3437-51C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_198576.4:c.3752-51C>T - intron variant - [Sequence Ontology: SO:0001627]