Canonical Allele Identifier: CA1405402039
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945635T= , CM000665.2:g.138945635T= GRCh38
NC_000003.11:g.138664477T= , CM000665.1:g.138664477T= GRCh37
NC_000003.10:g.140147167T= NCBI36
NG_012454.1:g.6506A=
NG_029796.1:g.3402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1088A= MANE Select ENSP00000497217.1:p.His363=
ENST00000330315.3:c.1088A= ENSP00000333188.3:p.His363=
NM_023067.3:c.1088A= NP_075555.1:p.His363=
NM_023067.4:c.1088A= MANE Select NP_075555.1:p.His363=
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