Canonical Allele Identifier: CA436094746
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1057516151
MyVariant Identifiers: chr3:g.138665262G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946420G>A , CM000665.2:g.138946420G>A GRCh38
NC_000003.11:g.138665262G>A , CM000665.1:g.138665262G>A GRCh37
NC_000003.10:g.140147952G>A NCBI36
NG_012454.1:g.5721C>T
NG_029796.1:g.4187G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.303C>T MANE Select ENSP00000497217.1:p.Ser101=
ENST00000330315.3:c.303C>T ENSP00000333188.3:p.Ser101=
NM_023067.3:c.303C>T NP_075555.1:p.Ser101=
NM_023067.4:c.303C>T MANE Select NP_075555.1:p.Ser101=