Canonical Allele Identifier: CA500450851

Gene: TBX21

Linked Data

• MyVariant Identifiers: chr17:g.45822177G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744811G>C , CM000679.2:g.47744811G>C	GRCh38
NC_000017.10:g.45822177G>C , CM000679.1:g.45822177G>C	GRCh37
NC_000017.9:g.43177176G>C	NCBI36
NG_012166.1:g.16568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1053G>C MANE Select	ENSP00000177694.1:p.Gly351=
ENST00000177694.1:c.1053G>C	ENSP00000177694.1:p.Gly351=
NM_013351.1:c.1053G>C	NP_037483.1:p.Gly351=
XM_011524698.1:c.1116G>C	XP_011523000.1:p.Gly372=
XM_011524699.1:c.720G>C	XP_011523001.1:p.Gly240=
NM_013351.2:c.1053G>C MANE Select	NP_037483.1:p.Gly351=