Canonical Allele Identifier: CA2262805741

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733684A= , CM000679.2:g.47733684A=	GRCh38
NC_000017.10:g.45811050A= , CM000679.1:g.45811050A=	GRCh37
NC_000017.9:g.43166049A=	NCBI36
NG_012166.1:g.5441A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.230A= MANE Select	ENSP00000177694.1:p.Tyr77=
ENST00000177694.1:c.230A=	ENSP00000177694.1:p.Tyr77=
ENST00000581328.1:n.260A=
NM_013351.1:c.230A=	NP_037483.1:p.Tyr77=
XM_011524698.1:c.230A=	XP_011523000.1:p.Tyr77=
NM_013351.2:c.230A= MANE Select	NP_037483.1:p.Tyr77=