Canonical Allele Identifier: CA10411760
Gene: FOXP3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2232368

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255822C>T , CM000685.2:g.49255822C>T GRCh38
NC_000023.10:g.49112283C>T , CM000685.1:g.49112283C>T GRCh37
NC_000023.9:g.48999227C>T NCBI36
NG_007392.1:g.14006G>A , LRG_62:g.14006G>A

Transcript Alleles

HGVS Amino-acid change
NM_001114377.1:c.543-20G>A VV NP_001107849.1:p.=
NM_014009.3:c.648-20G>A , LRG_62t1:c.648-20G>A NP_054728.2:p.=
XM_006724533.2:c.717-20G>A XP_006724596.2:p.=
XM_011543915.1:c.867-20G>A XP_011542217.1:p.=
XM_011543916.1:c.867-20G>A XP_011542218.1:p.=
XM_011543917.1:c.666-20G>A XP_011542219.1:p.=
XM_011543918.1:c.903-20G>A XP_011542220.1:p.=
XM_011543919.1:c.867-20G>A XP_011542221.1:p.=
XM_017029567.1:c.594-20G>A XP_016885056.1:p.=
ENST00000376197.1:n.498-20G>A ENSP00000365369.1:p.=
ENST00000376199.6:c.543-20G>A ENSP00000365372.2:p.=
ENST00000376207.8:c.648-20G>A ENSP00000365380.4:p.=
ENST00000455775.6:c.717-20G>A ENSP00000396415.3:p.=
ENST00000518685.5:c.543-20G>A ENSP00000428952.1:p.=
ENST00000557224.5:n.543-20G>A ENSP00000451208.1:p.=