Canonical Allele Identifier: CA500450973

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822213T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744847T>C , CM000679.2:g.47744847T>C	GRCh38
NC_000017.10:g.45822213T>C , CM000679.1:g.45822213T>C	GRCh37
NC_000017.9:g.43177212T>C	NCBI36
NG_012166.1:g.16604T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1089T>C MANE Select	ENSP00000177694.1:p.Tyr363=
ENST00000177694.1:c.1089T>C	ENSP00000177694.1:p.Tyr363=
NM_013351.1:c.1089T>C	NP_037483.1:p.Tyr363=
XM_011524698.1:c.1152T>C	XP_011523000.1:p.Tyr384=
XM_011524699.1:c.756T>C	XP_011523001.1:p.Tyr252=
NM_013351.2:c.1089T>C MANE Select	NP_037483.1:p.Tyr363=