Canonical Allele Identifier: CA354700681
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945666G>C , CM000665.2:g.138945666G>C GRCh38
NC_000003.11:g.138664508G>C , CM000665.1:g.138664508G>C GRCh37
NC_000003.10:g.140147198G>C NCBI36
NG_012454.1:g.6475C>G
NG_029796.1:g.3433G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1057C>G MANE Select ENSP00000497217.1:p.Leu353Val
ENST00000330315.3:c.1057C>G ENSP00000333188.3:p.Leu353Val
NM_023067.3:c.1057C>G NP_075555.1:p.Leu353Val
NM_023067.4:c.1057C>G MANE Select NP_075555.1:p.Leu353Val