Canonical Allele Identifier: CA1405402001
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945289G= , CM000665.2:g.138945289G= GRCh38
NC_000003.11:g.138664131G= , CM000665.1:g.138664131G= GRCh37
NC_000003.10:g.140146821G= NCBI36
NG_012454.1:g.6852C=
NG_029796.1:g.3056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*303C= MANE Select ENSP00000497217.1:n.*303C=
ENST00000330315.3:c.*303C= ENSP00000333188.3:n.*303C=
NM_023067.3:c.*303C= NP_075555.1:n.*303C=
NM_023067.4:c.*303C= MANE Select NP_075555.1:n.*303C=