Canonical Allele Identifier: CA400059829

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45811274C>T (hg19) ; chr17:g.47733908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47733908C>T , CM000679.2:g.47733908C>T	GRCh38
NC_000017.10:g.45811274C>T , CM000679.1:g.45811274C>T	GRCh37
NC_000017.9:g.43166273C>T	NCBI36
NG_012166.1:g.5665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.454C>T MANE Select	ENSP00000177694.1:p.Gln152Ter
ENST00000177694.1:c.454C>T	ENSP00000177694.1:p.Gln152Ter
ENST00000581328.1:n.484C>T
NM_013351.1:c.454C>T	NP_037483.1:p.Gln152Ter
XM_011524698.1:c.454C>T	XP_011523000.1:p.Gln152Ter
NM_013351.2:c.454C>T MANE Select	NP_037483.1:p.Gln152Ter