Canonical Allele Identifier: CA354700050
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107742982

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945602A>T , CM000665.2:g.138945602A>T GRCh38
NC_000003.11:g.138664444A>T , CM000665.1:g.138664444A>T GRCh37
NC_000003.10:g.140147134A>T NCBI36
NG_012454.1:g.6539T>A
NG_029796.1:g.3369A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1121T>A MANE Select ENSP00000497217.1:p.Leu374His
ENST00000330315.3:c.1121T>A ENSP00000333188.3:p.Leu374His
NM_023067.3:c.1121T>A NP_075555.1:p.Leu374His
NM_023067.4:c.1121T>A MANE Select NP_075555.1:p.Leu374His