ClinVar

NM_000258.3(MYL3):c.307+37A>C

Gene:

MYL3:myosin light chain 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p21.31

Genomic location:

• Chr3: 46860639 (on Assembly GRCh38)
• Chr3: 46902129 (on Assembly GRCh37)

Preferred name:

NM_000258.3(MYL3):c.307+37A>C

HGVS:

• NC_000003.12:g.46860639T>G
• NG_007555.2:g.26531A>C
• NM_000258.3:c.307+37A>CMANE SELECT
• LRG_395t1:c.307+37A>C
• LRG_395:g.26531A>C
• NC_000003.11:g.46902129T>G
• NM_000258.2:c.307+37A>C
• NM_000258.3:c.307+37A>C

This HGVS expression did not pass validation

Links:

dbSNP: rs2227294

NCBI 1000 Genomes Browser:

rs2227294

Molecular consequence:

• NM_000258.3:c.307+37A>C - intron variant - [Sequence Ontology: SO:0001627]