Canonical Allele Identifier: CA1405402024
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945325C= , CM000665.2:g.138945325C= GRCh38
NC_000003.11:g.138664167C= , CM000665.1:g.138664167C= GRCh37
NC_000003.10:g.140146857C= NCBI36
NG_012454.1:g.6816G=
NG_029796.1:g.3092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*267G= MANE Select ENSP00000497217.1:n.*267G=
ENST00000330315.3:c.*267G= ENSP00000333188.3:n.*267G=
NM_023067.3:c.*267G= NP_075555.1:n.*267G=
NM_023067.4:c.*267G= MANE Select NP_075555.1:n.*267G=