Canonical Allele Identifier: CA2262810701

Gene: TBX21

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47744775C= , CM000679.2:g.47744775C=	GRCh38
NC_000017.10:g.45822141C= , CM000679.1:g.45822141C=	GRCh37
NC_000017.9:g.43177140C=	NCBI36
NG_012166.1:g.16532C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000177694.2:c.1017C= MANE Select	ENSP00000177694.1:p.Ile339=
ENST00000177694.1:c.1017C=	ENSP00000177694.1:p.Ile339=
NM_013351.1:c.1017C=	NP_037483.1:p.Ile339=
XM_011524698.1:c.1080C=	XP_011523000.1:p.Ile360=
XM_011524699.1:c.684C=	XP_011523001.1:p.Ile228=
NM_013351.2:c.1017C= MANE Select	NP_037483.1:p.Ile339=