Canonical Allele Identifier: CA436094158
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107743358
MyVariant Identifiers: chr3:g.138664677T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945835T>G , CM000665.2:g.138945835T>G GRCh38
NC_000003.11:g.138664677T>G , CM000665.1:g.138664677T>G GRCh37
NC_000003.10:g.140147367T>G NCBI36
NG_012454.1:g.6306A>C
NG_029796.1:g.3602T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.888A>C MANE Select ENSP00000497217.1:p.Ala296=
ENST00000330315.3:c.888A>C ENSP00000333188.3:p.Ala296=
NM_023067.3:c.888A>C NP_075555.1:p.Ala296=
NM_023067.4:c.888A>C MANE Select NP_075555.1:p.Ala296=
Search 100 bp 5'
Search 100 bp 3'