Canonical Allele Identifier: CA354707677
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665402G>T (hg19) chr3:g.138946560G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946560G>T , CM000665.2:g.138946560G>T GRCh38
NC_000003.11:g.138665402G>T , CM000665.1:g.138665402G>T GRCh37
NC_000003.10:g.140148092G>T NCBI36
NG_012454.1:g.5581C>A
NG_029796.1:g.4327G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.163C>A MANE Select ENSP00000497217.1:p.Pro55Thr
ENST00000330315.3:c.163C>A ENSP00000333188.3:p.Pro55Thr
NM_023067.3:c.163C>A NP_075555.1:p.Pro55Thr
NM_023067.4:c.163C>A MANE Select NP_075555.1:p.Pro55Thr
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