LDH info

Canonical Allele Identifier: CA10654892
Gene: FOXL2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 369902
ClinVar RCV Id: RCV000408824
dbSNP Id: rs1057516153

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946412T>C , CM000665.2:g.138946412T>C GRCh38
NC_000003.11:g.138665254T>C , CM000665.1:g.138665254T>C GRCh37
NC_000003.10:g.140147944T>C NCBI36
NG_012454.1:g.5729A>G
NG_029796.1:g.4179T>C

Transcript Alleles

HGVS Amino-acid change
NM_023067.3:c.311A>G VV NP_075555.1:p.His104Arg
NM_023067.4:c.311A>G VV MANE Preferred NP_075555.1:p.His104Arg
ENST00000330315.3:c.311A>G ENSP00000333188.3:p.His104Arg