Canonical Allele Identifier: CA1405402014
Gene: FOXL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945622G= , CM000665.2:g.138945622G= GRCh38
NC_000003.11:g.138664464G= , CM000665.1:g.138664464G= GRCh37
NC_000003.10:g.140147154G= NCBI36
NG_012454.1:g.6519C=
NG_029796.1:g.3389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1101C= MANE Select ENSP00000497217.1:p.Thr367=
ENST00000330315.3:c.1101C= ENSP00000333188.3:p.Thr367=
NM_023067.3:c.1101C= NP_075555.1:p.Thr367=
NM_023067.4:c.1101C= MANE Select NP_075555.1:p.Thr367=
Search 100 bp 5'
Search 100 bp 3'