Canonical Allele Identifier: CA2262810694

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744751G= , CM000679.2:g.47744751G=	GRCh38
NC_000017.10:g.45822117G= , CM000679.1:g.45822117G=	GRCh37
NC_000017.9:g.43177116G=	NCBI36
NG_012166.1:g.16508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.993G= MANE Select	ENSP00000177694.1:p.Met331=
ENST00000177694.1:c.993G=	ENSP00000177694.1:p.Met331=
NM_013351.1:c.993G=	NP_037483.1:p.Met331=
XM_011524698.1:c.1056G=	XP_011523000.1:p.Met352=
XM_011524699.1:c.660G=	XP_011523001.1:p.Met220=
NM_013351.2:c.993G= MANE Select	NP_037483.1:p.Met331=