Canonical Allele Identifier: CA436094502
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935978314
MyVariant Identifiers: chr3:g.138665415G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946573G>A , CM000665.2:g.138946573G>A GRCh38
NC_000003.11:g.138665415G>A , CM000665.1:g.138665415G>A GRCh37
NC_000003.10:g.140148105G>A NCBI36
NG_012454.1:g.5568C>T
NG_029796.1:g.4340G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.150C>T MANE Select ENSP00000497217.1:p.Asp50=
ENST00000330315.3:c.150C>T ENSP00000333188.3:p.Asp50=
NM_023067.3:c.150C>T NP_075555.1:p.Asp50=
NM_023067.4:c.150C>T MANE Select NP_075555.1:p.Asp50=
Search 100 bp 5'
Search 100 bp 3'