Canonical Allele Identifier: CA2639779
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs768151902
ExAC: 3:138665178 C / T
gnomAD v2: 3-138665178-C-T
gnomAD v3: 3-138946336-C-T
gnomAD v4: 3-138946336-C-T
MyVariant Identifiers: chr3:g.138665178C>T (hg19) chr3:g.138946336C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946336C>T , CM000665.2:g.138946336C>T GRCh38
NC_000003.11:g.138665178C>T , CM000665.1:g.138665178C>T GRCh37
NC_000003.10:g.140147868C>T NCBI36
NG_012454.1:g.5805G>A
NG_029796.1:g.4103C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.387G>A MANE Select ENSP00000497217.1:p.Thr129=
ENST00000330315.3:c.387G>A ENSP00000333188.3:p.Thr129=
NM_023067.3:c.387G>A NP_075555.1:p.Thr129=
NM_023067.4:c.387G>A MANE Select NP_075555.1:p.Thr129=
Search 100 bp 5'
Search 100 bp 3'