LDH info

Canonical Allele Identifier: CA10588416
Gene: FOXC1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 265478
dbSNP Id: rs886039568

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610701C>T , CM000668.2:g.1610701C>T GRCh38
NC_000006.11:g.1610936C>T , CM000668.1:g.1610936C>T GRCh37
NC_000006.10:g.1555935C>T NCBI36
NG_009368.1:g.5256C>T

Transcript Alleles

HGVS Amino-acid change
NM_001453.2:n.256C>T VV NP_001444.2:p.Leu86Phe
NM_001453.3:c.256C>T VV NP_001444.2:p.Leu86Phe
ENST00000380874.3:c.256C>T ENSP00000370256.2:p.Leu86Phe