Canonical Allele Identifier: CA2262805826

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733852T= , CM000679.2:g.47733852T=	GRCh38
NC_000017.10:g.45811218T= , CM000679.1:g.45811218T=	GRCh37
NC_000017.9:g.43166217T=	NCBI36
NG_012166.1:g.5609T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000177694.2:c.398T= MANE Select	ENSP00000177694.1:p.Val133=
ENST00000177694.1:c.398T=	ENSP00000177694.1:p.Val133=
ENST00000581328.1:n.428T=
NM_013351.1:c.398T=	NP_037483.1:p.Val133=
XM_011524698.1:c.398T=	XP_011523000.1:p.Val133=
NM_013351.2:c.398T= MANE Select	NP_037483.1:p.Val133=