Canonical Allele Identifier: CA1405402347
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946106A= , CM000665.2:g.138946106A= GRCh38
NC_000003.11:g.138664948A= , CM000665.1:g.138664948A= GRCh37
NC_000003.10:g.140147638A= NCBI36
NG_012454.1:g.6035T=
NG_029796.1:g.3873A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.617T= MANE Select ENSP00000497217.1:p.Leu206=
ENST00000330315.3:c.617T= ENSP00000333188.3:p.Leu206=
NM_023067.3:c.617T= NP_075555.1:p.Leu206=
NM_023067.4:c.617T= MANE Select NP_075555.1:p.Leu206=