Canonical Allele Identifier: CA1405402227
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945911A= , CM000665.2:g.138945911A= GRCh38
NC_000003.11:g.138664753A= , CM000665.1:g.138664753A= GRCh37
NC_000003.10:g.140147443A= NCBI36
NG_012454.1:g.6230T=
NG_029796.1:g.3678A=

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.812T= MANE Select ENSP00000497217.1:p.Val271=
ENST00000330315.3:c.812T= ENSP00000333188.3:p.Val271=
NM_023067.3:c.812T= NP_075555.1:p.Val271=
NM_023067.4:c.812T= MANE Select NP_075555.1:p.Val271=