Canonical Allele Identifier: CA2639813
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2295040
ClinVar RCV Id: RCV002868303
dbSNP Id: rs758992234
ExAC: 3:138665455 C / T
gnomAD v2: 3-138665455-C-T
gnomAD v3: 3-138946613-C-T
gnomAD v4: 3-138946613-C-T
MyVariant Identifiers: chr3:g.138665455C>T (hg19) chr3:g.138946613C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946613C>T , CM000665.2:g.138946613C>T GRCh38
NC_000003.11:g.138665455C>T , CM000665.1:g.138665455C>T GRCh37
NC_000003.10:g.140148145C>T NCBI36
NG_012454.1:g.5528G>A
NG_029796.1:g.4380C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.110G>A MANE Select ENSP00000497217.1:p.Gly37Asp
ENST00000330315.3:c.110G>A ENSP00000333188.3:p.Gly37Asp
NM_023067.3:c.110G>A NP_075555.1:p.Gly37Asp
NM_023067.4:c.110G>A MANE Select NP_075555.1:p.Gly37Asp
Search 100 bp 5'
Search 100 bp 3'