Canonical Allele Identifier: CA436094610
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs768151902
MyVariant Identifiers: chr3:g.138665178C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946336C>G , CM000665.2:g.138946336C>G GRCh38
NC_000003.11:g.138665178C>G , CM000665.1:g.138665178C>G GRCh37
NC_000003.10:g.140147868C>G NCBI36
NG_012454.1:g.5805G>C
NG_029796.1:g.4103C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.387G>C MANE Select ENSP00000497217.1:p.Thr129=
ENST00000330315.3:c.387G>C ENSP00000333188.3:p.Thr129=
NM_023067.3:c.387G>C NP_075555.1:p.Thr129=
NM_023067.4:c.387G>C MANE Select NP_075555.1:p.Thr129=
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