Canonical Allele Identifier: CA513687486
Gene: TBX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19754345G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766822G>T , CM000684.2:g.19766822G>T GRCh38
NC_000022.10:g.19754345G>T , CM000684.1:g.19754345G>T GRCh37
NC_000022.9:g.18134345G>T NCBI36
NG_009229.1:g.15120G>T , LRG_226:g.15120G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1470G>T MANE Select ENSP00000497003.1:p.Ser490=
ENST00000329705.11:c.1009+820G>T ENSP00000331176.7:n.1009+820G>T
ENST00000332710.8:c.1443G>T ENSP00000331791.4:p.Ser481=
ENST00000359500.7:c.1009+820G>T ENSP00000352483.3:n.1009+820G>T
ENST00000621939.1:c.1009+820G>T ENSP00000477982.1:n.1009+820G>T
NM_005992.1:c.1009+820G>T NP_005983.1:n.1009+820G>T
NM_080646.1:c.1009+820G>T NP_542377.1:n.1009+820G>T
NM_080647.1:c.1443G>T , LRG_226t1:c.1443G>T NP_542378.1:p.Ser481=
XM_006724312.1:c.1443G>T XP_006724375.1:p.Ser481=
XM_011530351.1:c.1470G>T XP_011528653.1:p.Ser490=
XM_006724312.2:c.1443G>T XP_006724375.1:p.Ser481=
XM_017028925.1:c.1593G>T XP_016884414.1:p.Ser531=
XM_017028926.1:c.1443G>T XP_016884415.1:p.Ser481=
XM_017028927.1:c.798G>T XP_016884416.1:p.Ser266=
XM_017028928.1:c.1159+820G>T XP_016884417.1:n.1159+820G>T
NM_001379200.1:c.1470G>T MANE Select NP_001366129.1:p.Ser490=
NM_080646.2:c.1009+820G>T NP_542377.1:n.1009+820G>T