Canonical Allele Identifier: CA354706539
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665200T>G (hg19) chr3:g.138946358T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946358T>G , CM000665.2:g.138946358T>G GRCh38
NC_000003.11:g.138665200T>G , CM000665.1:g.138665200T>G GRCh37
NC_000003.10:g.140147890T>G NCBI36
NG_012454.1:g.5783A>C
NG_029796.1:g.4125T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.365A>C MANE Select ENSP00000497217.1:p.Glu122Ala
ENST00000330315.3:c.365A>C ENSP00000333188.3:p.Glu122Ala
NM_023067.3:c.365A>C NP_075555.1:p.Glu122Ala
NM_023067.4:c.365A>C MANE Select NP_075555.1:p.Glu122Ala
Search 100 bp 5'
Search 100 bp 3'