Canonical Allele Identifier: CA329133873

Gene: FOXP3

Linked Data

• dbSNP Id: rs187780818
• gnomAD v3: X-49251967-G-A
• gnomAD v4: X-49251967-G-A
• MyVariant Identifiers: chrX:g.49108428G>A (hg19) ; chrX:g.49251967G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251967G>A , CM000685.2:g.49251967G>A	GRCh38
NC_000023.10:g.49108428G>A , CM000685.1:g.49108428G>A	GRCh37
NC_000023.9:g.48995372G>A	NCBI36
NG_007392.1:g.17861C>T , LRG_62:g.17861C>T
NG_021311.2:g.21503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-202C>T	ENSP00000365372.2:n.940-202C>T
ENST00000376207.10:c.1045-202C>T MANE Select	ENSP00000365380.4:n.1045-202C>T
ENST00000455775.7:c.1114-202C>T	ENSP00000396415.3:n.1114-202C>T
ENST00000518685.6:c.964-202C>T	ENSP00000428952.2:n.964-202C>T
ENST00000557224.6:c.940-202C>T	ENSP00000451208.1:n.940-202C>T
ENST00000651307.1:c.968-202C>T	ENSP00000498454.1:n.968-202C>T
ENST00000376197.1:c.895-202C>T	ENSP00000365369.1:n.895-202C>T
ENST00000376199.6:c.940-202C>T	ENSP00000365372.2:n.940-202C>T
ENST00000376207.8:c.1045-202C>T	ENSP00000365380.4:n.1045-202C>T
ENST00000455775.6:c.1114-202C>T	ENSP00000396415.3:n.1114-202C>T
ENST00000518685.5:c.940-202C>T	ENSP00000428952.1:n.940-202C>T
ENST00000557224.5:c.940-202C>T	ENSP00000451208.1:n.940-202C>T
NM_001114377.1:c.940-202C>T	NP_001107849.1:n.940-202C>T
NM_014009.3:c.1045-202C>T , LRG_62t1:c.1045-202C>T	NP_054728.2:n.1045-202C>T
XM_006724533.2:c.1114-202C>T	XP_006724596.2:n.1114-202C>T
XM_011543915.1:c.1264-202C>T	XP_011542217.1:n.1264-202C>T
XM_011543916.1:c.1264-202C>T	XP_011542218.1:n.1264-202C>T
XM_011543917.1:c.1063-202C>T	XP_011542219.1:n.1063-202C>T
XM_011543918.1:c.1300-202C>T	XP_011542220.1:n.1300-202C>T
XM_011543919.1:c.1264-202C>T	XP_011542221.1:n.1264-202C>T
XM_017029567.1:c.991-202C>T	XP_016885056.1:n.991-202C>T
NM_001114377.2:c.940-202C>T	NP_001107849.1:n.940-202C>T
NM_014009.4:c.1045-202C>T MANE Select	NP_054728.2:n.1045-202C>T