Canonical Allele Identifier: CA2639784
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs121908358

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946428G>T , CM000665.2:g.138946428G>T GRCh38
NC_000003.11:g.138665270G>T , CM000665.1:g.138665270G>T GRCh37
NC_000003.10:g.140147960G>T NCBI36
NG_012454.1:g.5713C>A
NG_029796.1:g.4195G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.295C>A MANE Select ENSP00000497217.1:p.Gln99Lys
ENST00000330315.3:c.295C>A ENSP00000333188.3:p.Gln99Lys
NM_023067.3:c.295C>A NP_075555.1:p.Gln99Lys
NM_023067.4:c.295C>A MANE Select NP_075555.1:p.Gln99Lys