Canonical Allele Identifier: CA400059574

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45811248A>T (hg19) ; chr17:g.47733882A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733882A>T , CM000679.2:g.47733882A>T	GRCh38
NC_000017.10:g.45811248A>T , CM000679.1:g.45811248A>T	GRCh37
NC_000017.9:g.43166247A>T	NCBI36
NG_012166.1:g.5639A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.428A>T MANE Select	ENSP00000177694.1:p.Asn143Ile
ENST00000177694.1:c.428A>T	ENSP00000177694.1:p.Asn143Ile
ENST00000581328.1:n.458A>T
NM_013351.1:c.428A>T	NP_037483.1:p.Asn143Ile
XM_011524698.1:c.428A>T	XP_011523000.1:p.Asn143Ile
NM_013351.2:c.428A>T MANE Select	NP_037483.1:p.Asn143Ile