Canonical Allele Identifier: CA2638459237
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733435-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733435A>G , CM000679.2:g.47733435A>G GRCh38
NC_000017.10:g.45810801A>G , CM000679.1:g.45810801A>G GRCh37
NC_000017.9:g.43165800A>G NCBI36
NG_012166.1:g.5192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-20A>G MANE Select ENSP00000177694.1:n.-20A>G
ENST00000177694.1:c.-20A>G ENSP00000177694.1:n.-20A>G
ENST00000581328.1:n.11A>G
NM_013351.1:c.-20A>G NP_037483.1:n.-20A>G
XM_011524698.1:c.-20A>G XP_011523000.1:n.-20A>G
NM_013351.2:c.-20A>G MANE Select NP_037483.1:n.-20A>G
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