Canonical Allele Identifier: CA1405402501
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946420G= , CM000665.2:g.138946420G= GRCh38
NC_000003.11:g.138665262G= , CM000665.1:g.138665262G= GRCh37
NC_000003.10:g.140147952G= NCBI36
NG_012454.1:g.5721C=
NG_029796.1:g.4187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.303C= MANE Select ENSP00000497217.1:p.Ser101=
ENST00000330315.3:c.303C= ENSP00000333188.3:p.Ser101=
NM_023067.3:c.303C= NP_075555.1:p.Ser101=
NM_023067.4:c.303C= MANE Select NP_075555.1:p.Ser101=