Canonical Allele Identifier: CA436094330
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107744075
MyVariant Identifiers: chr3:g.138665010G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946168G>C , CM000665.2:g.138946168G>C GRCh38
NC_000003.11:g.138665010G>C , CM000665.1:g.138665010G>C GRCh37
NC_000003.10:g.140147700G>C NCBI36
NG_012454.1:g.5973C>G
NG_029796.1:g.3935G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.555C>G MANE Select ENSP00000497217.1:p.Gly185=
ENST00000330315.3:c.555C>G ENSP00000333188.3:p.Gly185=
NM_023067.3:c.555C>G NP_075555.1:p.Gly185=
NM_023067.4:c.555C>G MANE Select NP_075555.1:p.Gly185=
Search 100 bp 5'
Search 100 bp 3'