Canonical Allele Identifier: CA354706889
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946420G>T , CM000665.2:g.138946420G>T GRCh38
NC_000003.11:g.138665262G>T , CM000665.1:g.138665262G>T GRCh37
NC_000003.10:g.140147952G>T NCBI36
NG_012454.1:g.5721C>A
NG_029796.1:g.4187G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.303C>A MANE Select ENSP00000497217.1:p.Ser101Arg
ENST00000330315.3:c.303C>A ENSP00000333188.3:p.Ser101Arg
NM_023067.3:c.303C>A NP_075555.1:p.Ser101Arg
NM_023067.4:c.303C>A MANE Select NP_075555.1:p.Ser101Arg