Canonical Allele Identifier: CA500450782

Gene: TBX21

Linked Data

• gnomAD v4: 17-47744790-A-T
• MyVariant Identifiers: chr17:g.45822156A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744790A>T , CM000679.2:g.47744790A>T	GRCh38
NC_000017.10:g.45822156A>T , CM000679.1:g.45822156A>T	GRCh37
NC_000017.9:g.43177155A>T	NCBI36
NG_012166.1:g.16547A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1032A>T MANE Select	ENSP00000177694.1:p.Gly344=
ENST00000177694.1:c.1032A>T	ENSP00000177694.1:p.Gly344=
NM_013351.1:c.1032A>T	NP_037483.1:p.Gly344=
XM_011524698.1:c.1095A>T	XP_011523000.1:p.Gly365=
XM_011524699.1:c.699A>T	XP_011523001.1:p.Gly233=
NM_013351.2:c.1032A>T MANE Select	NP_037483.1:p.Gly344=