Canonical Allele Identifier: CA500449462
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45810835G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733469G>A , CM000679.2:g.47733469G>A GRCh38
NC_000017.10:g.45810835G>A , CM000679.1:g.45810835G>A GRCh37
NC_000017.9:g.43165834G>A NCBI36
NG_012166.1:g.5226G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.15G>A MANE Select ENSP00000177694.1:p.Glu5=
ENST00000177694.1:c.15G>A ENSP00000177694.1:p.Glu5=
ENST00000581328.1:n.45G>A
NM_013351.1:c.15G>A NP_037483.1:p.Glu5=
XM_011524698.1:c.15G>A XP_011523000.1:p.Glu5=
NM_013351.2:c.15G>A MANE Select NP_037483.1:p.Glu5=