Canonical Allele Identifier: CA1405402205
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945865A= , CM000665.2:g.138945865A= GRCh38
NC_000003.11:g.138664707A= , CM000665.1:g.138664707A= GRCh37
NC_000003.10:g.140147397A= NCBI36
NG_012454.1:g.6276T=
NG_029796.1:g.3632A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.858T= MANE Select ENSP00000497217.1:p.Pro286=
ENST00000330315.3:c.858T= ENSP00000333188.3:p.Pro286=
NM_023067.3:c.858T= NP_075555.1:p.Pro286=
NM_023067.4:c.858T= MANE Select NP_075555.1:p.Pro286=