Canonical Allele Identifier: CA354706870
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107744725

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946418A>G , CM000665.2:g.138946418A>G GRCh38
NC_000003.11:g.138665260A>G , CM000665.1:g.138665260A>G GRCh37
NC_000003.10:g.140147950A>G NCBI36
NG_012454.1:g.5723T>C
NG_029796.1:g.4185A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.305T>C MANE Select ENSP00000497217.1:p.Ile102Thr
ENST00000330315.3:c.305T>C ENSP00000333188.3:p.Ile102Thr
NM_023067.3:c.305T>C NP_075555.1:p.Ile102Thr
NM_023067.4:c.305T>C MANE Select NP_075555.1:p.Ile102Thr