Canonical Allele Identifier: CA1405401750
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945455G= , CM000665.2:g.138945455G= GRCh38
NC_000003.11:g.138664297G= , CM000665.1:g.138664297G= GRCh37
NC_000003.10:g.140146987G= NCBI36
NG_012454.1:g.6686C=
NG_029796.1:g.3222G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*137C= MANE Select ENSP00000497217.1:n.*137C=
ENST00000330315.3:c.*137C= ENSP00000333188.3:n.*137C=
NM_023067.3:c.*137C= NP_075555.1:n.*137C=
NM_023067.4:c.*137C= MANE Select NP_075555.1:n.*137C=