Canonical Allele Identifier: CA292260291

Gene: TBX4

Linked Data

• dbSNP Id: rs545321990
• gnomAD v3: 17-61455994-G-A
• gnomAD v4: 17-61455994-G-A
• MyVariant Identifiers: chr17:g.59533355G>A (hg19) ; chr17:g.61455994G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61455994G>A , CM000679.2:g.61455994G>A	GRCh38
NC_000017.10:g.59533355G>A , CM000679.1:g.59533355G>A	GRCh37
NC_000017.9:g.56888137G>A	NCBI36
NG_008080.1:g.4549G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644296.1:c.-3-494G>A MANE Select	ENSP00000495986.1:n.-3-494G>A
ENST00000393853.8:c.-3-494G>A	ENSP00000377435.3:n.-3-494G>A
ENST00000589003.5:c.-125-630G>A	ENSP00000467588.1:n.-125-630G>A
XM_005257835.3:c.-3-494G>A	XP_005257892.2:n.-3-494G>A
XM_005257837.2:c.-3-494G>A	XP_005257894.1:n.-3-494G>A
XM_011525490.1:c.187-494G>A	XP_011523792.1:n.187-494G>A
XM_011525491.1:c.187-494G>A	XP_011523793.1:n.187-494G>A
XM_011525492.1:c.-3-494G>A	XP_011523794.1:n.-3-494G>A
XM_011525493.1:c.-3-494G>A	XP_011523795.1:n.-3-494G>A
XM_011525494.1:c.-4+259G>A	XP_011523796.1:n.-4+259G>A
XM_011525495.1:c.187-494G>A	XP_011523797.1:n.187-494G>A
NM_001321120.2:c.-3-494G>A MANE Select	NP_001308049.1:n.-3-494G>A
XM_011525490.2:c.187-494G>A	XP_011523792.1:n.187-494G>A
XM_011525491.2:c.187-494G>A	XP_011523793.1:n.187-494G>A
XM_011525495.2:c.187-494G>A	XP_011523797.1:n.187-494G>A