ClinVar

NM_153646.4(SLC24A4):c.1051-35T>C

Gene:

SLC24A4:solute carrier family 24 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.12

Genomic location:

• Chr14: 92456369 (on Assembly GRCh38)
• Chr14: 92922713 (on Assembly GRCh37)

Preferred name:

NM_153646.4(SLC24A4):c.1051-35T>C

HGVS:

• NC_000014.9:g.92456369T>C
• NG_023408.1:g.138789T>C
• NM_001378620.1:c.1051-35T>C
• NM_153646.4:c.1051-35T>CMANE SELECT
• NM_153647.4:c.994-35T>C
• NM_153648.4:c.859-35T>C
• NC_000014.8:g.92922713T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs7158400

NCBI 1000 Genomes Browser:

rs7158400

Molecular consequence:

• NM_001378620.1:c.1051-35T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_153646.4:c.1051-35T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_153647.4:c.994-35T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_153648.4:c.859-35T>C - intron variant - [Sequence Ontology: SO:0001627]