Canonical Allele Identifier: CA1405402584
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946593T= , CM000665.2:g.138946593T= GRCh38
NC_000003.11:g.138665435T= , CM000665.1:g.138665435T= GRCh37
NC_000003.10:g.140148125T= NCBI36
NG_012454.1:g.5548A=
NG_029796.1:g.4360T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.130A= MANE Select ENSP00000497217.1:p.Thr44=
ENST00000330315.3:c.130A= ENSP00000333188.3:p.Thr44=
NM_023067.3:c.130A= NP_075555.1:p.Thr44=
NM_023067.4:c.130A= MANE Select NP_075555.1:p.Thr44=
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