Canonical Allele Identifier: CA354706899
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2813999
ClinVar RCV Id: RCV003680727
dbSNP Id: rs2107744740
MyVariant Identifiers: chr3:g.138665263C>G (hg19) chr3:g.138946421C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946421C>G , CM000665.2:g.138946421C>G GRCh38
NC_000003.11:g.138665263C>G , CM000665.1:g.138665263C>G GRCh37
NC_000003.10:g.140147953C>G NCBI36
NG_012454.1:g.5720G>C
NG_029796.1:g.4188C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.302G>C MANE Select ENSP00000497217.1:p.Ser101Thr
ENST00000330315.3:c.302G>C ENSP00000333188.3:p.Ser101Thr
NM_023067.3:c.302G>C NP_075555.1:p.Ser101Thr
NM_023067.4:c.302G>C MANE Select NP_075555.1:p.Ser101Thr
Search 100 bp 5'
Search 100 bp 3'