Canonical Allele Identifier: CA2262805674

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733566C= , CM000679.2:g.47733566C=	GRCh38
NC_000017.10:g.45810932C= , CM000679.1:g.45810932C=	GRCh37
NC_000017.9:g.43165931C=	NCBI36
NG_012166.1:g.5323C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000177694.2:c.112C= MANE Select	ENSP00000177694.1:p.Pro38=
ENST00000177694.1:c.112C=	ENSP00000177694.1:p.Pro38=
ENST00000581328.1:n.142C=
NM_013351.1:c.112C=	NP_037483.1:p.Pro38=
XM_011524698.1:c.112C=	XP_011523000.1:p.Pro38=
NM_013351.2:c.112C= MANE Select	NP_037483.1:p.Pro38=