Canonical Allele Identifier: CA400058961

Gene: TBX21

Linked Data

• dbSNP Id: rs2032170294
• MyVariant Identifiers: chr17:g.45811145G>T (hg19) ; chr17:g.47733779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733779G>T , CM000679.2:g.47733779G>T	GRCh38
NC_000017.10:g.45811145G>T , CM000679.1:g.45811145G>T	GRCh37
NC_000017.9:g.43166144G>T	NCBI36
NG_012166.1:g.5536G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.325G>T MANE Select	ENSP00000177694.1:p.Ala109Ser
ENST00000177694.1:c.325G>T	ENSP00000177694.1:p.Ala109Ser
ENST00000581328.1:n.355G>T
NM_013351.1:c.325G>T	NP_037483.1:p.Ala109Ser
XM_011524698.1:c.325G>T	XP_011523000.1:p.Ala109Ser
NM_013351.2:c.325G>T MANE Select	NP_037483.1:p.Ala109Ser