Canonical Allele Identifier: CA1405402019
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945624T= , CM000665.2:g.138945624T= GRCh38
NC_000003.11:g.138664466T= , CM000665.1:g.138664466T= GRCh37
NC_000003.10:g.140147156T= NCBI36
NG_012454.1:g.6517A=
NG_029796.1:g.3391T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1099A= MANE Select ENSP00000497217.1:p.Thr367=
ENST00000330315.3:c.1099A= ENSP00000333188.3:p.Thr367=
NM_023067.3:c.1099A= NP_075555.1:p.Thr367=
NM_023067.4:c.1099A= MANE Select NP_075555.1:p.Thr367=
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