Canonical Allele Identifier: CA2262805596

Gene: TBX21

Linked Data

• dbSNP Id: rs2032162053

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733410_47733411insAA , CM000679.2:g.47733410_47733411insAA	GRCh38
NC_000017.10:g.45810776_45810777insAA , CM000679.1:g.45810776_45810777insAA	GRCh37
NC_000017.9:g.43165775_43165776insAA	NCBI36
NG_012166.1:g.5167_5168insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.-45_-44insAA MANE Select	ENSP00000177694.1:n.-45_-44insAA
ENST00000177694.1:c.-45_-44insAA	ENSP00000177694.1:n.-45_-44insAA
NM_013351.1:c.-45_-44insAA	NP_037483.1:n.-45_-44insAA
XM_011524698.1:c.-45_-44insAA	XP_011523000.1:n.-45_-44insAA
NM_013351.2:c.-45_-44insAA MANE Select	NP_037483.1:n.-45_-44insAA