Canonical Allele Identifier: CA1405402214
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945884G= , CM000665.2:g.138945884G= GRCh38
NC_000003.11:g.138664726G= , CM000665.1:g.138664726G= GRCh37
NC_000003.10:g.140147416G= NCBI36
NG_012454.1:g.6257C=
NG_029796.1:g.3651G=

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.839C= MANE Select ENSP00000497217.1:p.Pro280=
ENST00000330315.3:c.839C= ENSP00000333188.3:p.Pro280=
NM_023067.3:c.839C= NP_075555.1:p.Pro280=
NM_023067.4:c.839C= MANE Select NP_075555.1:p.Pro280=