Canonical Allele Identifier: CA1405402038
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945339G= , CM000665.2:g.138945339G= GRCh38
NC_000003.11:g.138664181G= , CM000665.1:g.138664181G= GRCh37
NC_000003.10:g.140146871G= NCBI36
NG_012454.1:g.6802C=
NG_029796.1:g.3106G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*253C= MANE Select ENSP00000497217.1:n.*253C=
ENST00000330315.3:c.*253C= ENSP00000333188.3:n.*253C=
NM_023067.3:c.*253C= NP_075555.1:n.*253C=
NM_023067.4:c.*253C= MANE Select NP_075555.1:n.*253C=