Canonical Allele Identifier: CA354706915
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1356397966

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946423A>C , CM000665.2:g.138946423A>C GRCh38
NC_000003.11:g.138665265A>C , CM000665.1:g.138665265A>C GRCh37
NC_000003.10:g.140147955A>C NCBI36
NG_012454.1:g.5718T>G
NG_029796.1:g.4190A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.300T>G MANE Select ENSP00000497217.1:p.Asn100Lys
ENST00000330315.3:c.300T>G ENSP00000333188.3:p.Asn100Lys
NM_023067.3:c.300T>G NP_075555.1:p.Asn100Lys
NM_023067.4:c.300T>G MANE Select NP_075555.1:p.Asn100Lys