Canonical Allele Identifier: CA1405402361
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946141G= , CM000665.2:g.138946141G= GRCh38
NC_000003.11:g.138664983G= , CM000665.1:g.138664983G= GRCh37
NC_000003.10:g.140147673G= NCBI36
NG_012454.1:g.6000C=
NG_029796.1:g.3908G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.582C= MANE Select ENSP00000497217.1:p.Tyr194=
ENST00000330315.3:c.582C= ENSP00000333188.3:p.Tyr194=
NM_023067.3:c.582C= NP_075555.1:p.Tyr194=
NM_023067.4:c.582C= MANE Select NP_075555.1:p.Tyr194=