Canonical Allele Identifier: CA354704605
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1057516168
MyVariant Identifiers: chr3:g.138664921T>A (hg19) chr3:g.138946079T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946079T>A , CM000665.2:g.138946079T>A GRCh38
NC_000003.11:g.138664921T>A , CM000665.1:g.138664921T>A GRCh37
NC_000003.10:g.140147611T>A NCBI36
NG_012454.1:g.6062A>T
NG_029796.1:g.3846T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.644A>T MANE Select ENSP00000497217.1:p.Tyr215Phe
ENST00000330315.3:c.644A>T ENSP00000333188.3:p.Tyr215Phe
NM_023067.3:c.644A>T NP_075555.1:p.Tyr215Phe
NM_023067.4:c.644A>T MANE Select NP_075555.1:p.Tyr215Phe
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