Canonical Allele Identifier: CA83969226
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs930127232
MyVariant Identifiers: chr3:g.138664218G>A (hg19) chr3:g.138945376G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945376G>A , CM000665.2:g.138945376G>A GRCh38
NC_000003.11:g.138664218G>A , CM000665.1:g.138664218G>A GRCh37
NC_000003.10:g.140146908G>A NCBI36
NG_012454.1:g.6765C>T
NG_029796.1:g.3143G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*216C>T MANE Select ENSP00000497217.1:n.*216C>T
ENST00000330315.3:c.*216C>T ENSP00000333188.3:n.*216C>T
NM_023067.3:c.*216C>T NP_075555.1:n.*216C>T
NM_023067.4:c.*216C>T MANE Select NP_075555.1:n.*216C>T
Search 100 bp 5'
Search 100 bp 3'