Canonical Allele Identifier: CA500652565
Gene: TBX21 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45811123C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733757C>A , CM000679.2:g.47733757C>A GRCh38
NC_000017.10:g.45811123C>A , CM000679.1:g.45811123C>A GRCh37
NC_000017.9:g.43166122C>A NCBI36
NG_012166.1:g.5514C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.303C>A MANE Select ENSP00000177694.1:p.Gly101=
ENST00000177694.1:c.303C>A ENSP00000177694.1:p.Gly101=
ENST00000581328.1:n.333C>A
NM_013351.1:c.303C>A NP_037483.1:p.Gly101=
XM_011524698.1:c.303C>A XP_011523000.1:p.Gly101=
NM_013351.2:c.303C>A MANE Select NP_037483.1:p.Gly101=
Search 100 bp 5'
Search 100 bp 3'