Canonical Allele Identifier: CA354704794
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946098G>C , CM000665.2:g.138946098G>C GRCh38
NC_000003.11:g.138664940G>C , CM000665.1:g.138664940G>C GRCh37
NC_000003.10:g.140147630G>C NCBI36
NG_012454.1:g.6043C>G
NG_029796.1:g.3865G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.625C>G MANE Select ENSP00000497217.1:p.Pro209Ala
ENST00000330315.3:c.625C>G ENSP00000333188.3:p.Pro209Ala
NM_023067.3:c.625C>G NP_075555.1:p.Pro209Ala
NM_023067.4:c.625C>G MANE Select NP_075555.1:p.Pro209Ala