Canonical Allele Identifier: CA354706884
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107744727

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946419T>G , CM000665.2:g.138946419T>G GRCh38
NC_000003.11:g.138665261T>G , CM000665.1:g.138665261T>G GRCh37
NC_000003.10:g.140147951T>G NCBI36
NG_012454.1:g.5722A>C
NG_029796.1:g.4186T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.304A>C MANE Select ENSP00000497217.1:p.Ile102Leu
ENST00000330315.3:c.304A>C ENSP00000333188.3:p.Ile102Leu
NM_023067.3:c.304A>C NP_075555.1:p.Ile102Leu
NM_023067.4:c.304A>C MANE Select NP_075555.1:p.Ile102Leu