Canonical Allele Identifier: CA410685077

Gene: TBX1

Linked Data

• ClinVar Variation Id: 1417829
• ClinVar RCV Id: RCV001938641 ; RCV002386731
• dbSNP Id: rs1177085596
• gnomAD v2: 22-19754221-G-A
• gnomAD v4: 22-19766698-G-A
• MyVariant Identifiers: chr22:g.19754221G>A (hg19) ; chr22:g.19766698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766698G>A , CM000684.2:g.19766698G>A	GRCh38
NC_000022.10:g.19754221G>A , CM000684.1:g.19754221G>A	GRCh37
NC_000022.9:g.18134221G>A	NCBI36
NG_009229.1:g.14996G>A , LRG_226:g.14996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.1346G>A MANE Select	ENSP00000497003.1:p.Gly449Asp
ENST00000329705.11:c.1009+696G>A	ENSP00000331176.7:n.1009+696G>A
ENST00000332710.8:c.1319G>A	ENSP00000331791.4:p.Gly440Asp
ENST00000359500.7:c.1009+696G>A	ENSP00000352483.3:n.1009+696G>A
ENST00000621939.1:c.1009+696G>A	ENSP00000477982.1:n.1009+696G>A
NM_005992.1:c.1009+696G>A	NP_005983.1:n.1009+696G>A
NM_080646.1:c.1009+696G>A	NP_542377.1:n.1009+696G>A
NM_080647.1:c.1319G>A , LRG_226t1:c.1319G>A	NP_542378.1:p.Gly440Asp
XM_006724312.1:c.1319G>A	XP_006724375.1:p.Gly440Asp
XM_011530351.1:c.1346G>A	XP_011528653.1:p.Gly449Asp
XM_006724312.2:c.1319G>A	XP_006724375.1:p.Gly440Asp
XM_017028925.1:c.1469G>A	XP_016884414.1:p.Gly490Asp
XM_017028926.1:c.1319G>A	XP_016884415.1:p.Gly440Asp
XM_017028927.1:c.674G>A	XP_016884416.1:p.Gly225Asp
XM_017028928.1:c.1159+696G>A	XP_016884417.1:n.1159+696G>A
NM_001379200.1:c.1346G>A MANE Select	NP_001366129.1:p.Gly449Asp
NM_080646.2:c.1009+696G>A	NP_542377.1:n.1009+696G>A