Canonical Allele Identifier: CA875961732

Gene: FOXP3

Linked Data

• dbSNP Id: rs2232366
• gnomAD v3: X-49258209-C-G
• gnomAD v4: X-49258209-C-G
• MyVariant Identifiers: chrX:g.49114666C>G (hg19) ; chrX:g.49258209C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49258209C>G , CM000685.2:g.49258209C>G	GRCh38
NC_000023.10:g.49114666C>G , CM000685.1:g.49114666C>G	GRCh37
NC_000023.9:g.49001610C>G	NCBI36
NG_007392.1:g.11623G>C , LRG_62:g.11623G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684155.1:c.210+87G>C	ENSP00000507726.1:n.210+87G>C
ENST00000376199.7:c.210+87G>C	ENSP00000365372.2:n.210+87G>C
ENST00000376207.10:c.210+87G>C MANE Select	ENSP00000365380.4:n.210+87G>C
ENST00000455775.7:c.210+87G>C	ENSP00000396415.3:n.210+87G>C
ENST00000518685.6:c.210+87G>C	ENSP00000428952.2:n.210+87G>C
ENST00000557224.6:c.210+87G>C	ENSP00000451208.1:n.210+87G>C
ENST00000651307.1:c.210+87G>C	ENSP00000498454.1:n.210+87G>C
ENST00000652559.1:c.210+87G>C	ENSP00000498236.1:n.210+87G>C
ENST00000376197.1:c.165+87G>C	ENSP00000365369.1:n.165+87G>C
ENST00000376199.6:c.210+87G>C	ENSP00000365372.2:n.210+87G>C
ENST00000376207.8:c.210+87G>C	ENSP00000365380.4:n.210+87G>C
ENST00000455775.6:c.210+87G>C	ENSP00000396415.3:n.210+87G>C
ENST00000518685.5:c.210+87G>C	ENSP00000428952.1:n.210+87G>C
ENST00000557224.5:c.210+87G>C	ENSP00000451208.1:n.210+87G>C
NM_001114377.1:c.210+87G>C	NP_001107849.1:n.210+87G>C
NM_014009.3:c.210+87G>C , LRG_62t1:c.210+87G>C	NP_054728.2:n.210+87G>C
XM_006724533.2:c.210+87G>C	XP_006724596.2:n.210+87G>C
XM_011543915.1:c.534+87G>C	XP_011542217.1:n.534+87G>C
XM_011543916.1:c.534+87G>C	XP_011542218.1:n.534+87G>C
XM_011543917.1:c.210+87G>C	XP_011542219.1:n.210+87G>C
XM_011543918.1:c.534+87G>C	XP_011542220.1:n.534+87G>C
XM_011543919.1:c.534+87G>C	XP_011542221.1:n.534+87G>C
XM_017029567.1:c.261+87G>C	XP_016885056.1:n.261+87G>C
NM_001114377.2:c.210+87G>C	NP_001107849.1:n.210+87G>C
NM_014009.4:c.210+87G>C MANE Select	NP_054728.2:n.210+87G>C