Canonical Allele Identifier: CA400050438

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822178G>T (hg19) ; chr17:g.47744812G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744812G>T , CM000679.2:g.47744812G>T	GRCh38
NC_000017.10:g.45822178G>T , CM000679.1:g.45822178G>T	GRCh37
NC_000017.9:g.43177177G>T	NCBI36
NG_012166.1:g.16569G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1054G>T MANE Select	ENSP00000177694.1:p.Gly352Ter
ENST00000177694.1:c.1054G>T	ENSP00000177694.1:p.Gly352Ter
NM_013351.1:c.1054G>T	NP_037483.1:p.Gly352Ter
XM_011524698.1:c.1117G>T	XP_011523000.1:p.Gly373Ter
XM_011524699.1:c.721G>T	XP_011523001.1:p.Gly241Ter
NM_013351.2:c.1054G>T MANE Select	NP_037483.1:p.Gly352Ter