Canonical Allele Identifier: CA354707120
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665302A>T (hg19) chr3:g.138946460A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946460A>T , CM000665.2:g.138946460A>T GRCh38
NC_000003.11:g.138665302A>T , CM000665.1:g.138665302A>T GRCh37
NC_000003.10:g.140147992A>T NCBI36
NG_012454.1:g.5681T>A
NG_029796.1:g.4227A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.263T>A MANE Select ENSP00000497217.1:p.Phe88Tyr
ENST00000330315.3:c.263T>A ENSP00000333188.3:p.Phe88Tyr
NM_023067.3:c.263T>A NP_075555.1:p.Phe88Tyr
NM_023067.4:c.263T>A MANE Select NP_075555.1:p.Phe88Tyr
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