Canonical Allele Identifier: CA436094112
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1245058278
MyVariant Identifiers: chr3:g.138664647C>G (hg19) chr3:g.138945805C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945805C>G , CM000665.2:g.138945805C>G GRCh38
NC_000003.11:g.138664647C>G , CM000665.1:g.138664647C>G GRCh37
NC_000003.10:g.140147337C>G NCBI36
NG_012454.1:g.6336G>C
NG_029796.1:g.3572C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.918G>C MANE Select ENSP00000497217.1:p.Pro306=
ENST00000330315.3:c.918G>C ENSP00000333188.3:p.Pro306=
NM_023067.3:c.918G>C NP_075555.1:p.Pro306=
NM_023067.4:c.918G>C MANE Select NP_075555.1:p.Pro306=
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