Canonical Allele Identifier: CA2639789
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs752795632
ExAC: 3:138665315 T / C
gnomAD v4: 3-138946473-T-C
MyVariant Identifiers: chr3:g.138665315T>C (hg19) chr3:g.138946473T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946473T>C , CM000665.2:g.138946473T>C GRCh38
NC_000003.11:g.138665315T>C , CM000665.1:g.138665315T>C GRCh37
NC_000003.10:g.140148005T>C NCBI36
NG_012454.1:g.5668A>G
NG_029796.1:g.4240T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.250A>G MANE Select ENSP00000497217.1:p.Ile84Val
ENST00000330315.3:c.250A>G ENSP00000333188.3:p.Ile84Val
NM_023067.3:c.250A>G NP_075555.1:p.Ile84Val
NM_023067.4:c.250A>G MANE Select NP_075555.1:p.Ile84Val
Search 100 bp 5'
Search 100 bp 3'