Canonical Allele Identifier: CA354704472
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935960053
MyVariant Identifiers: chr3:g.138664906A>C (hg19) chr3:g.138946064A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946064A>C , CM000665.2:g.138946064A>C GRCh38
NC_000003.11:g.138664906A>C , CM000665.1:g.138664906A>C GRCh37
NC_000003.10:g.140147596A>C NCBI36
NG_012454.1:g.6077T>G
NG_029796.1:g.3831A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.659T>G MANE Select ENSP00000497217.1:p.Met220Arg
ENST00000330315.3:c.659T>G ENSP00000333188.3:p.Met220Arg
NM_023067.3:c.659T>G NP_075555.1:p.Met220Arg
NM_023067.4:c.659T>G MANE Select NP_075555.1:p.Met220Arg
Search 100 bp 5'
Search 100 bp 3'