Canonical Allele Identifier: CA354708183
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107745035

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946635G>A , CM000665.2:g.138946635G>A GRCh38
NC_000003.11:g.138665477G>A , CM000665.1:g.138665477G>A GRCh37
NC_000003.10:g.140148167G>A NCBI36
NG_012454.1:g.5506C>T
NG_029796.1:g.4402G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.88C>T MANE Select ENSP00000497217.1:p.Pro30Ser
ENST00000330315.3:c.88C>T ENSP00000333188.3:p.Pro30Ser
NM_023067.3:c.88C>T NP_075555.1:p.Pro30Ser
NM_023067.4:c.88C>T MANE Select NP_075555.1:p.Pro30Ser