Canonical Allele Identifier: CA354700237
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1157290194
MyVariant Identifiers: chr3:g.138664471C>A (hg19) chr3:g.138945629C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945629C>A , CM000665.2:g.138945629C>A GRCh38
NC_000003.11:g.138664471C>A , CM000665.1:g.138664471C>A GRCh37
NC_000003.10:g.140147161C>A NCBI36
NG_012454.1:g.6512G>T
NG_029796.1:g.3396C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1094G>T MANE Select ENSP00000497217.1:p.Ser365Ile
ENST00000330315.3:c.1094G>T ENSP00000333188.3:p.Ser365Ile
NM_023067.3:c.1094G>T NP_075555.1:p.Ser365Ile
NM_023067.4:c.1094G>T MANE Select NP_075555.1:p.Ser365Ile
Search 100 bp 5'
Search 100 bp 3'