Canonical Allele Identifier: CA436094200
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935959530
gnomAD v4: 3-138946051-T-C
MyVariant Identifiers: chr3:g.138664893T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946051T>C , CM000665.2:g.138946051T>C GRCh38
NC_000003.11:g.138664893T>C , CM000665.1:g.138664893T>C GRCh37
NC_000003.10:g.140147583T>C NCBI36
NG_012454.1:g.6090A>G
NG_029796.1:g.3818T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.672A>G MANE Select ENSP00000497217.1:p.Ala224=
ENST00000330315.3:c.672A>G ENSP00000333188.3:p.Ala224=
NM_023067.3:c.672A>G NP_075555.1:p.Ala224=
NM_023067.4:c.672A>G MANE Select NP_075555.1:p.Ala224=
Search 100 bp 5'
Search 100 bp 3'