Canonical Allele Identifier: CA2639771
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs781285704
ExAC: 3:138665127 G / C
gnomAD v2: 3-138665127-G-C
gnomAD v3: 3-138946285-G-C
gnomAD v4: 3-138946285-G-C
COSMIC: COSM4113959
MyVariant Identifiers: chr3:g.138665127G>C (hg19) chr3:g.138946285G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946285G>C , CM000665.2:g.138946285G>C GRCh38
NC_000003.11:g.138665127G>C , CM000665.1:g.138665127G>C GRCh37
NC_000003.10:g.140147817G>C NCBI36
NG_012454.1:g.5856C>G
NG_029796.1:g.4052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.438C>G MANE Select ENSP00000497217.1:p.Arg146=
ENST00000330315.3:c.438C>G ENSP00000333188.3:p.Arg146=
NM_023067.3:c.438C>G NP_075555.1:p.Arg146=
NM_023067.4:c.438C>G MANE Select NP_075555.1:p.Arg146=
Search 100 bp 5'
Search 100 bp 3'