Canonical Allele Identifier: CA354706895
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946421C>A , CM000665.2:g.138946421C>A GRCh38
NC_000003.11:g.138665263C>A , CM000665.1:g.138665263C>A GRCh37
NC_000003.10:g.140147953C>A NCBI36
NG_012454.1:g.5720G>T
NG_029796.1:g.4188C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.302G>T MANE Select ENSP00000497217.1:p.Ser101Ile
ENST00000330315.3:c.302G>T ENSP00000333188.3:p.Ser101Ile
NM_023067.3:c.302G>T NP_075555.1:p.Ser101Ile
NM_023067.4:c.302G>T MANE Select NP_075555.1:p.Ser101Ile