Canonical Allele Identifier: CA354704649
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107743834
MyVariant Identifiers: chr3:g.138664925G>C (hg19) chr3:g.138946083G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946083G>C , CM000665.2:g.138946083G>C GRCh38
NC_000003.11:g.138664925G>C , CM000665.1:g.138664925G>C GRCh37
NC_000003.10:g.140147615G>C NCBI36
NG_012454.1:g.6058C>G
NG_029796.1:g.3850G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.640C>G MANE Select ENSP00000497217.1:p.Pro214Ala
ENST00000330315.3:c.640C>G ENSP00000333188.3:p.Pro214Ala
NM_023067.3:c.640C>G NP_075555.1:p.Pro214Ala
NM_023067.4:c.640C>G MANE Select NP_075555.1:p.Pro214Ala
Search 100 bp 5'
Search 100 bp 3'