Canonical Allele Identifier: CA500450822

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822168A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744802A>G , CM000679.2:g.47744802A>G	GRCh38
NC_000017.10:g.45822168A>G , CM000679.1:g.45822168A>G	GRCh37
NC_000017.9:g.43177167A>G	NCBI36
NG_012166.1:g.16559A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1044A>G MANE Select	ENSP00000177694.1:p.Gln348=
ENST00000177694.1:c.1044A>G	ENSP00000177694.1:p.Gln348=
NM_013351.1:c.1044A>G	NP_037483.1:p.Gln348=
XM_011524698.1:c.1107A>G	XP_011523000.1:p.Gln369=
XM_011524699.1:c.711A>G	XP_011523001.1:p.Gln237=
NM_013351.2:c.1044A>G MANE Select	NP_037483.1:p.Gln348=