Canonical Allele Identifier: CA354708312
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107745088
MyVariant Identifiers: chr3:g.138665507T>G (hg19) chr3:g.138946665T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946665T>G , CM000665.2:g.138946665T>G GRCh38
NC_000003.11:g.138665507T>G , CM000665.1:g.138665507T>G GRCh37
NC_000003.10:g.140148197T>G NCBI36
NG_012454.1:g.5476A>C
NG_029796.1:g.4432T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.58A>C MANE Select ENSP00000497217.1:p.Thr20Pro
ENST00000330315.3:c.58A>C ENSP00000333188.3:p.Thr20Pro
NM_023067.3:c.58A>C NP_075555.1:p.Thr20Pro
NM_023067.4:c.58A>C MANE Select NP_075555.1:p.Thr20Pro
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