Canonical Allele Identifier: CA2262805619
Gene: TBX21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733456_47733457delinsTG , CM000679.2:g.47733456_47733457delinsTG GRCh38
NC_000017.10:g.45810822_45810823delinsTG , CM000679.1:g.45810822_45810823delinsTG GRCh37
NC_000017.9:g.43165821_43165822delinsTG NCBI36
NG_012166.1:g.5213_5214delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.2_3delinsTG MANE Select ENSP00000177694.1:p.Met1=
ENST00000177694.1:c.2_3delinsTG ENSP00000177694.1:p.Met1=
ENST00000581328.1:n.32_33delinsTG
NM_013351.1:c.2_3delinsTG NP_037483.1:p.Met1=
XM_011524698.1:c.2_3delinsTG XP_011523000.1:p.Met1=
NM_013351.2:c.2_3delinsTG MANE Select NP_037483.1:p.Met1=