Canonical Allele Identifier: CA354708141
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107745021

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946626T>C , CM000665.2:g.138946626T>C GRCh38
NC_000003.11:g.138665468T>C , CM000665.1:g.138665468T>C GRCh37
NC_000003.10:g.140148158T>C NCBI36
NG_012454.1:g.5515A>G
NG_029796.1:g.4393T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.97A>G MANE Select ENSP00000497217.1:p.Ser33Gly
ENST00000330315.3:c.97A>G ENSP00000333188.3:p.Ser33Gly
NM_023067.3:c.97A>G NP_075555.1:p.Ser33Gly
NM_023067.4:c.97A>G MANE Select NP_075555.1:p.Ser33Gly