Canonical Allele Identifier: CA354706971
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1057516150

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946430C>G , CM000665.2:g.138946430C>G GRCh38
NC_000003.11:g.138665272C>G , CM000665.1:g.138665272C>G GRCh37
NC_000003.10:g.140147962C>G NCBI36
NG_012454.1:g.5711G>C
NG_029796.1:g.4197C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.293G>C MANE Select ENSP00000497217.1:p.Trp98Ser
ENST00000330315.3:c.293G>C ENSP00000333188.3:p.Trp98Ser
NM_023067.3:c.293G>C NP_075555.1:p.Trp98Ser
NM_023067.4:c.293G>C MANE Select NP_075555.1:p.Trp98Ser