Canonical Allele Identifier: CA500450693

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822129T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744763T>A , CM000679.2:g.47744763T>A	GRCh38
NC_000017.10:g.45822129T>A , CM000679.1:g.45822129T>A	GRCh37
NC_000017.9:g.43177128T>A	NCBI36
NG_012166.1:g.16520T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1005T>A MANE Select	ENSP00000177694.1:p.Val335=
ENST00000177694.1:c.1005T>A	ENSP00000177694.1:p.Val335=
NM_013351.1:c.1005T>A	NP_037483.1:p.Val335=
XM_011524698.1:c.1068T>A	XP_011523000.1:p.Val356=
XM_011524699.1:c.672T>A	XP_011523001.1:p.Val224=
NM_013351.2:c.1005T>A MANE Select	NP_037483.1:p.Val335=