Canonical Allele Identifier: CA2638459038
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733353G>C , CM000679.2:g.47733353G>C GRCh38
NC_000017.10:g.45810719G>C , CM000679.1:g.45810719G>C GRCh37
NC_000017.9:g.43165718G>C NCBI36
NG_012166.1:g.5110G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-102G>C MANE Select ENSP00000177694.1:n.-102G>C
ENST00000177694.1:c.-102G>C ENSP00000177694.1:n.-102G>C
NM_013351.1:c.-102G>C NP_037483.1:n.-102G>C
XM_011524698.1:c.-102G>C XP_011523000.1:n.-102G>C
NM_013351.2:c.-102G>C MANE Select NP_037483.1:n.-102G>C