Canonical Allele Identifier: CA436094173
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138946033-C-T
MyVariant Identifiers: chr3:g.138664875C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946033C>T , CM000665.2:g.138946033C>T GRCh38
NC_000003.11:g.138664875C>T , CM000665.1:g.138664875C>T GRCh37
NC_000003.10:g.140147565C>T NCBI36
NG_012454.1:g.6108G>A
NG_029796.1:g.3800C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.690G>A MANE Select ENSP00000497217.1:p.Ala230=
ENST00000330315.3:c.690G>A ENSP00000333188.3:p.Ala230=
NM_023067.3:c.690G>A NP_075555.1:p.Ala230=
NM_023067.4:c.690G>A MANE Select NP_075555.1:p.Ala230=
Search 100 bp 5'
Search 100 bp 3'