Canonical Allele Identifier: CA354706977
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1057516149
MyVariant Identifiers: chr3:g.138665273A>T (hg19) chr3:g.138946431A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946431A>T , CM000665.2:g.138946431A>T GRCh38
NC_000003.11:g.138665273A>T , CM000665.1:g.138665273A>T GRCh37
NC_000003.10:g.140147963A>T NCBI36
NG_012454.1:g.5710T>A
NG_029796.1:g.4198A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.292T>A MANE Select ENSP00000497217.1:p.Trp98Arg
ENST00000330315.3:c.292T>A ENSP00000333188.3:p.Trp98Arg
NM_023067.3:c.292T>A NP_075555.1:p.Trp98Arg
NM_023067.4:c.292T>A MANE Select NP_075555.1:p.Trp98Arg
Search 100 bp 5'
Search 100 bp 3'