Canonical Allele Identifier: CA14436277
Community Standard Title: NM_013351.2(TBX21):c.*303G>A
Gene: TBX21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47745669G>A , CM000679.2:g.47745669G>A GRCh38
NC_000017.10:g.45823035G>A , CM000679.1:g.45823035G>A GRCh37
NC_000017.9:g.43178034G>A NCBI36
NG_012166.1:g.17426G>A

Transcript Alleles

HGVS Amino-acid Change
NM_013351.2:c.*303G>A MANE Select NP_037483.1:n.*303G>A
ENST00000177694.2:c.*303G>A MANE Select ENSP00000177694.1:n.*303G>A
NM_013351.1:c.*303G>A NP_037483.1:n.*303G>A
ENST00000177694.1:c.*303G>A ENSP00000177694.1:n.*303G>A
XM_011524698.1:c.*303G>A XP_011523000.1:n.*303G>A
XM_011524699.1:c.*303G>A XP_011523001.1:n.*303G>A
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