Canonical Allele Identifier: CA400059785

Gene: TBX21

Linked Data

• COSMIC: COSM5706432
• MyVariant Identifiers: chr17:g.45811268T>G (hg19) ; chr17:g.47733902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733902T>G , CM000679.2:g.47733902T>G	GRCh38
NC_000017.10:g.45811268T>G , CM000679.1:g.45811268T>G	GRCh37
NC_000017.9:g.43166267T>G	NCBI36
NG_012166.1:g.5659T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.448T>G MANE Select	ENSP00000177694.1:p.Phe150Val
ENST00000177694.1:c.448T>G	ENSP00000177694.1:p.Phe150Val
ENST00000581328.1:n.478T>G
NM_013351.1:c.448T>G	NP_037483.1:p.Phe150Val
XM_011524698.1:c.448T>G	XP_011523000.1:p.Phe150Val
NM_013351.2:c.448T>G MANE Select	NP_037483.1:p.Phe150Val