Canonical Allele Identifier: CA436094192
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107743395
MyVariant Identifiers: chr3:g.138664701C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945859C>G , CM000665.2:g.138945859C>G GRCh38
NC_000003.11:g.138664701C>G , CM000665.1:g.138664701C>G GRCh37
NC_000003.10:g.140147391C>G NCBI36
NG_012454.1:g.6282G>C
NG_029796.1:g.3626C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.864G>C MANE Select ENSP00000497217.1:p.Pro288=
ENST00000330315.3:c.864G>C ENSP00000333188.3:p.Pro288=
NM_023067.3:c.864G>C NP_075555.1:p.Pro288=
NM_023067.4:c.864G>C MANE Select NP_075555.1:p.Pro288=
Search 100 bp 5'
Search 100 bp 3'