Canonical Allele Identifier: CA354700581
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1340809159
MyVariant Identifiers: chr3:g.138664499T>C (hg19) chr3:g.138945657T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945657T>C , CM000665.2:g.138945657T>C GRCh38
NC_000003.11:g.138664499T>C , CM000665.1:g.138664499T>C GRCh37
NC_000003.10:g.140147189T>C NCBI36
NG_012454.1:g.6484A>G
NG_029796.1:g.3424T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1066A>G MANE Select ENSP00000497217.1:p.Met356Val
ENST00000330315.3:c.1066A>G ENSP00000333188.3:p.Met356Val
NM_023067.3:c.1066A>G NP_075555.1:p.Met356Val
NM_023067.4:c.1066A>G MANE Select NP_075555.1:p.Met356Val
Search 100 bp 5'
Search 100 bp 3'