Canonical Allele Identifier: CA500450879

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822186C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744820C>T , CM000679.2:g.47744820C>T	GRCh38
NC_000017.10:g.45822186C>T , CM000679.1:g.45822186C>T	GRCh37
NC_000017.9:g.43177185C>T	NCBI36
NG_012166.1:g.16577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1062C>T MANE Select	ENSP00000177694.1:p.His354=
ENST00000177694.1:c.1062C>T	ENSP00000177694.1:p.His354=
NM_013351.1:c.1062C>T	NP_037483.1:p.His354=
XM_011524698.1:c.1125C>T	XP_011523000.1:p.His375=
XM_011524699.1:c.729C>T	XP_011523001.1:p.His243=
NM_013351.2:c.1062C>T MANE Select	NP_037483.1:p.His354=