Canonical Allele Identifier: CA400059366
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs1597981301
gnomAD v4: 17-47733852-T-G
MyVariant Identifiers: chr17:g.45811218T>G (hg19) chr17:g.47733852T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733852T>G , CM000679.2:g.47733852T>G GRCh38
NC_000017.10:g.45811218T>G , CM000679.1:g.45811218T>G GRCh37
NC_000017.9:g.43166217T>G NCBI36
NG_012166.1:g.5609T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.398T>G MANE Select ENSP00000177694.1:p.Val133Gly
ENST00000177694.1:c.398T>G ENSP00000177694.1:p.Val133Gly
ENST00000581328.1:n.428T>G
NM_013351.1:c.398T>G NP_037483.1:p.Val133Gly
XM_011524698.1:c.398T>G XP_011523000.1:p.Val133Gly
NM_013351.2:c.398T>G MANE Select NP_037483.1:p.Val133Gly
Search 100 bp 5'
Search 100 bp 3'