Canonical Allele Identifier: CA354708216
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107745051

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946643G>C , CM000665.2:g.138946643G>C GRCh38
NC_000003.11:g.138665485G>C , CM000665.1:g.138665485G>C GRCh37
NC_000003.10:g.140148175G>C NCBI36
NG_012454.1:g.5498C>G
NG_029796.1:g.4410G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.80C>G MANE Select ENSP00000497217.1:p.Pro27Arg
ENST00000330315.3:c.80C>G ENSP00000333188.3:p.Pro27Arg
NM_023067.3:c.80C>G NP_075555.1:p.Pro27Arg
NM_023067.4:c.80C>G MANE Select NP_075555.1:p.Pro27Arg