Canonical Allele Identifier: CA2638459039
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733354T>G , CM000679.2:g.47733354T>G GRCh38
NC_000017.10:g.45810720T>G , CM000679.1:g.45810720T>G GRCh37
NC_000017.9:g.43165719T>G NCBI36
NG_012166.1:g.5111T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-101T>G MANE Select ENSP00000177694.1:n.-101T>G
ENST00000177694.1:c.-101T>G ENSP00000177694.1:n.-101T>G
NM_013351.1:c.-101T>G NP_037483.1:n.-101T>G
XM_011524698.1:c.-101T>G XP_011523000.1:n.-101T>G
NM_013351.2:c.-101T>G MANE Select NP_037483.1:n.-101T>G