Canonical Allele Identifier: CA354702672
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1200776119
gnomAD v3: 3-138945855-G-A
gnomAD v4: 3-138945855-G-A
MyVariant Identifiers: chr3:g.138664697G>A (hg19) chr3:g.138945855G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945855G>A , CM000665.2:g.138945855G>A GRCh38
NC_000003.11:g.138664697G>A , CM000665.1:g.138664697G>A GRCh37
NC_000003.10:g.140147387G>A NCBI36
NG_012454.1:g.6286C>T
NG_029796.1:g.3622G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.868C>T MANE Select ENSP00000497217.1:p.Pro290Ser
ENST00000330315.3:c.868C>T ENSP00000333188.3:p.Pro290Ser
NM_023067.3:c.868C>T NP_075555.1:p.Pro290Ser
NM_023067.4:c.868C>T MANE Select NP_075555.1:p.Pro290Ser
Search 100 bp 5'
Search 100 bp 3'