Canonical Allele Identifier: CA354706944
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946426T>A , CM000665.2:g.138946426T>A GRCh38
NC_000003.11:g.138665268T>A , CM000665.1:g.138665268T>A GRCh37
NC_000003.10:g.140147958T>A NCBI36
NG_012454.1:g.5715A>T
NG_029796.1:g.4193T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.297A>T MANE Select ENSP00000497217.1:p.Gln99His
ENST00000330315.3:c.297A>T ENSP00000333188.3:p.Gln99His
NM_023067.3:c.297A>T NP_075555.1:p.Gln99His
NM_023067.4:c.297A>T MANE Select NP_075555.1:p.Gln99His