Canonical Allele Identifier: CA1405402033
Gene: FOXL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945633C= , CM000665.2:g.138945633C= GRCh38
NC_000003.11:g.138664475C= , CM000665.1:g.138664475C= GRCh37
NC_000003.10:g.140147165C= NCBI36
NG_012454.1:g.6508G=
NG_029796.1:g.3400C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1090G= MANE Select ENSP00000497217.1:p.Asp364=
ENST00000330315.3:c.1090G= ENSP00000333188.3:p.Asp364=
NM_023067.3:c.1090G= NP_075555.1:p.Asp364=
NM_023067.4:c.1090G= MANE Select NP_075555.1:p.Asp364=
Search 100 bp 5'
Search 100 bp 3'