Canonical Allele Identifier: CA400057227
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733473-G-T
MyVariant Identifiers: chr17:g.45810839G>T (hg19) chr17:g.47733473G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733473G>T , CM000679.2:g.47733473G>T GRCh38
NC_000017.10:g.45810839G>T , CM000679.1:g.45810839G>T GRCh37
NC_000017.9:g.43165838G>T NCBI36
NG_012166.1:g.5230G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.19G>T MANE Select ENSP00000177694.1:p.Gly7Cys
ENST00000177694.1:c.19G>T ENSP00000177694.1:p.Gly7Cys
ENST00000581328.1:n.49G>T
NM_013351.1:c.19G>T NP_037483.1:p.Gly7Cys
XM_011524698.1:c.19G>T XP_011523000.1:p.Gly7Cys
NM_013351.2:c.19G>T MANE Select NP_037483.1:p.Gly7Cys
Search 100 bp 5'
Search 100 bp 3'