Canonical Allele Identifier: CA1405402022
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935927119
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945316A>T , CM000665.2:g.138945316A>T GRCh38
NC_000003.11:g.138664158A>T , CM000665.1:g.138664158A>T GRCh37
NC_000003.10:g.140146848A>T NCBI36
NG_012454.1:g.6825T>A
NG_029796.1:g.3083A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*276T>A MANE Select ENSP00000497217.1:n.*276T>A
ENST00000330315.3:c.*276T>A ENSP00000333188.3:n.*276T>A
NM_023067.3:c.*276T>A NP_075555.1:n.*276T>A
NM_023067.4:c.*276T>A MANE Select NP_075555.1:n.*276T>A
Search 100 bp 5'
Search 100 bp 3'