Canonical Allele Identifier: CA386863575

Gene: TBX5

Linked Data

• dbSNP Id: rs1444078249
• gnomAD v3: 12-114403834-A-C
• gnomAD v4: 12-114403834-A-C
• MyVariant Identifiers: chr12:g.114841639A>C (hg19) ; chr12:g.114403834A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403834A>C , CM000674.2:g.114403834A>C	GRCh38
NC_000012.11:g.114841639A>C , CM000674.1:g.114841639A>C	GRCh37
NC_000012.10:g.113326022A>C	NCBI36
NG_007373.1:g.9609T>G , LRG_670:g.9609T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.65T>G MANE Select	ENSP00000384152.3:p.Leu22Arg
ENST00000310346.8:c.65T>G	ENSP00000309913.4:p.Leu22Arg
ENST00000349716.9:c.-3-1914T>G	ENSP00000337723.5:n.-3-1914T>G
ENST00000405440.6:c.65T>G	ENSP00000384152.2:p.Leu22Arg
ENST00000526441.1:c.65T>G	ENSP00000433292.1:p.Leu22Arg
ENST00000552726.1:n.116T>G
NM_000192.3:c.65T>G , LRG_670t1:c.65T>G	NP_000183.2:p.Leu22Arg
NM_080717.2:c.-3-1914T>G	NP_542448.1:n.-3-1914T>G
NM_181486.2:c.65T>G	NP_852259.1:p.Leu22Arg
XM_017019912.1:c.113T>G	XP_016875401.1:p.Leu38Arg
NM_080717.3:c.-3-1914T>G	NP_542448.1:n.-3-1914T>G
NM_181486.4:c.65T>G MANE Select	NP_852259.1:p.Leu22Arg
NM_080717.4:c.-3-1914T>G	NP_542448.1:n.-3-1914T>G