Canonical Allele Identifier: CA1132982635
Gene: FOXP3 HGNC NCBI

Linked Data

dbSNP Id: rs2066111528
gnomAD v3: X-49261724-G-T
gnomAD v4: X-49261724-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49261724G>T , CM000685.2:g.49261724G>T GRCh38
NC_000023.10:g.49118181G>T , CM000685.1:g.49118181G>T GRCh37
NC_000023.9:g.49005125G>T NCBI36
NG_007392.1:g.8108C>A , LRG_62:g.8108C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703450.1:c.-22-3197C>A ENSP00000515301.1:n.-22-3197C>A
ENST00000684155.1:c.-23+2937C>A ENSP00000507726.1:n.-23+2937C>A
ENST00000376199.7:c.-23+2937C>A ENSP00000365372.2:n.-23+2937C>A
ENST00000376207.10:c.-23+2937C>A MANE Select ENSP00000365380.4:n.-23+2937C>A
ENST00000455775.7:c.-23+2937C>A ENSP00000396415.3:n.-23+2937C>A
ENST00000557224.6:c.-23+2937C>A ENSP00000451208.1:n.-23+2937C>A
ENST00000650877.1:c.-22-3197C>A ENSP00000499100.1:n.-22-3197C>A
ENST00000652559.1:c.-23+2937C>A ENSP00000498236.1:n.-23+2937C>A
ENST00000376199.6:c.-23+2937C>A ENSP00000365372.2:n.-23+2937C>A
ENST00000376207.8:c.-23+2937C>A ENSP00000365380.4:n.-23+2937C>A
ENST00000455775.6:c.-23+2937C>A ENSP00000396415.3:n.-23+2937C>A
NM_001114377.1:c.-23+2937C>A NP_001107849.1:n.-23+2937C>A
NM_014009.3:c.-23+2937C>A , LRG_62t1:c.-23+2937C>A NP_054728.2:n.-23+2937C>A
XM_006724533.2:c.-23+2937C>A XP_006724596.2:n.-23+2937C>A
XM_011543915.1:c.302+2937C>A XP_011542217.1:n.302+2937C>A
XM_011543916.1:c.302+2937C>A XP_011542218.1:n.302+2937C>A
XM_011543917.1:c.-23+2937C>A XP_011542219.1:n.-23+2937C>A
XM_011543918.1:c.302+2937C>A XP_011542220.1:n.302+2937C>A
XM_011543919.1:c.302+2937C>A XP_011542221.1:n.302+2937C>A
XM_017029567.1:c.29+2807C>A XP_016885056.1:n.29+2807C>A
NM_001114377.2:c.-23+2937C>A NP_001107849.1:n.-23+2937C>A
NM_014009.4:c.-23+2937C>A MANE Select NP_054728.2:n.-23+2937C>A