Canonical Allele Identifier: CA354700731
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935940513
gnomAD v4: 3-138945673-C-A
MyVariant Identifiers: chr3:g.138664515C>A (hg19) chr3:g.138945673C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945673C>A , CM000665.2:g.138945673C>A GRCh38
NC_000003.11:g.138664515C>A , CM000665.1:g.138664515C>A GRCh37
NC_000003.10:g.140147205C>A NCBI36
NG_012454.1:g.6468G>T
NG_029796.1:g.3440C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1050G>T MANE Select ENSP00000497217.1:p.Gln350His
ENST00000330315.3:c.1050G>T ENSP00000333188.3:p.Gln350His
NM_023067.3:c.1050G>T NP_075555.1:p.Gln350His
NM_023067.4:c.1050G>T MANE Select NP_075555.1:p.Gln350His
Search 100 bp 5'
Search 100 bp 3'