Canonical Allele Identifier: CA2639719
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs767284567
ExAC: 3:138664744 T / C
gnomAD v2: 3-138664744-T-C
gnomAD v4: 3-138945902-T-C
MyVariant Identifiers: chr3:g.138664744T>C (hg19) chr3:g.138945902T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945902T>C , CM000665.2:g.138945902T>C GRCh38
NC_000003.11:g.138664744T>C , CM000665.1:g.138664744T>C GRCh37
NC_000003.10:g.140147434T>C NCBI36
NG_012454.1:g.6239A>G
NG_029796.1:g.3669T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.821A>G MANE Select ENSP00000497217.1:p.Tyr274Cys
ENST00000330315.3:c.821A>G ENSP00000333188.3:p.Tyr274Cys
NM_023067.3:c.821A>G NP_075555.1:p.Tyr274Cys
NM_023067.4:c.821A>G MANE Select NP_075555.1:p.Tyr274Cys
Search 100 bp 5'
Search 100 bp 3'