Canonical Allele Identifier: CA2439980782
Gene: TBX22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80026864A= , CM000685.2:g.80026864A= GRCh38
NC_000023.10:g.79282363A= , CM000685.1:g.79282363A= GRCh37
NC_000023.9:g.79169019A= NCBI36
NG_008998.1:g.17109A=

Transcript Alleles

HGVS Amino-acid change
ENST00000373296.8:c.794A= MANE Select ENSP00000362393.3:p.Gln265=
ENST00000373294.8:c.794A= ENSP00000362390.5:p.Gln265=
ENST00000373296.7:c.794A= ENSP00000362393.3:p.Gln265=
ENST00000626498.2:c.*406A= ENSP00000487527.1:n.*406A=
ENST00000626877.1:n.673A=
NM_001109878.1:c.794A= NP_001103348.1:p.Gln265=
NM_001109879.1:c.434A= NP_001103349.1:p.Gln145=
NM_001303475.1:c.434A= NP_001290404.1:p.Gln145=
NM_016954.2:c.794A= NP_058650.1:p.Gln265=
XM_005262136.2:c.797A= XP_005262193.1:p.Gln266=
XM_006724657.2:c.797A= XP_006724720.1:p.Gln266=
XM_011530972.1:c.434A= XP_011529274.1:p.Gln145=
NM_001109878.2:c.794A= MANE Select NP_001103348.1:p.Gln265=
NM_001109879.2:c.434A= NP_001103349.1:p.Gln145=