Canonical Allele Identifier: CA354707798
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665414G>T (hg19) chr3:g.138946572G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946572G>T , CM000665.2:g.138946572G>T GRCh38
NC_000003.11:g.138665414G>T , CM000665.1:g.138665414G>T GRCh37
NC_000003.10:g.140148104G>T NCBI36
NG_012454.1:g.5569C>A
NG_029796.1:g.4339G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.151C>A MANE Select ENSP00000497217.1:p.Pro51Thr
ENST00000330315.3:c.151C>A ENSP00000333188.3:p.Pro51Thr
NM_023067.3:c.151C>A NP_075555.1:p.Pro51Thr
NM_023067.4:c.151C>A MANE Select NP_075555.1:p.Pro51Thr
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