Canonical Allele Identifier: CA2639681
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs757838701

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945611T>G , CM000665.2:g.138945611T>G GRCh38
NC_000003.11:g.138664453T>G , CM000665.1:g.138664453T>G GRCh37
NC_000003.10:g.140147143T>G NCBI36
NG_012454.1:g.6530A>C
NG_029796.1:g.3378T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1112A>C MANE Select ENSP00000497217.1:p.His371Pro
ENST00000330315.3:c.1112A>C ENSP00000333188.3:p.His371Pro
NM_023067.3:c.1112A>C NP_075555.1:p.His371Pro
NM_023067.4:c.1112A>C MANE Select NP_075555.1:p.His371Pro