Canonical Allele Identifier: CA2262810698

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744764G= , CM000679.2:g.47744764G=	GRCh38
NC_000017.10:g.45822130G= , CM000679.1:g.45822130G=	GRCh37
NC_000017.9:g.43177129G=	NCBI36
NG_012166.1:g.16521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1006G= MANE Select	ENSP00000177694.1:p.Asp336=
ENST00000177694.1:c.1006G=	ENSP00000177694.1:p.Asp336=
NM_013351.1:c.1006G=	NP_037483.1:p.Asp336=
XM_011524698.1:c.1069G=	XP_011523000.1:p.Asp357=
XM_011524699.1:c.673G=	XP_011523001.1:p.Asp225=
NM_013351.2:c.1006G= MANE Select	NP_037483.1:p.Asp336=