Canonical Allele Identifier: CA436094564
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107745081
gnomAD v4: 3-138946660-A-G
MyVariant Identifiers: chr3:g.138665502A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946660A>G , CM000665.2:g.138946660A>G GRCh38
NC_000003.11:g.138665502A>G , CM000665.1:g.138665502A>G GRCh37
NC_000003.10:g.140148192A>G NCBI36
NG_012454.1:g.5481T>C
NG_029796.1:g.4427A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.63T>C MANE Select ENSP00000497217.1:p.Gly21=
ENST00000330315.3:c.63T>C ENSP00000333188.3:p.Gly21=
NM_023067.3:c.63T>C NP_075555.1:p.Gly21=
NM_023067.4:c.63T>C MANE Select NP_075555.1:p.Gly21=
Search 100 bp 5'
Search 100 bp 3'