Canonical Allele Identifier: CA354700902
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138664531A>C (hg19) chr3:g.138945689A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945689A>C , CM000665.2:g.138945689A>C GRCh38
NC_000003.11:g.138664531A>C , CM000665.1:g.138664531A>C GRCh37
NC_000003.10:g.140147221A>C NCBI36
NG_012454.1:g.6452T>G
NG_029796.1:g.3456A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1034T>G MANE Select ENSP00000497217.1:p.Phe345Cys
ENST00000330315.3:c.1034T>G ENSP00000333188.3:p.Phe345Cys
NM_023067.3:c.1034T>G NP_075555.1:p.Phe345Cys
NM_023067.4:c.1034T>G MANE Select NP_075555.1:p.Phe345Cys
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