Canonical Allele Identifier: CA500449523
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs1783360493
gnomAD v3: 17-47733556-C-T
gnomAD v4: 17-47733556-C-T
MyVariant Identifiers: chr17:g.45810922C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733556C>T , CM000679.2:g.47733556C>T GRCh38
NC_000017.10:g.45810922C>T , CM000679.1:g.45810922C>T GRCh37
NC_000017.9:g.43165921C>T NCBI36
NG_012166.1:g.5313C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000177694.2:c.102C>T MANE Select ENSP00000177694.1:p.Arg34=
ENST00000177694.1:c.102C>T ENSP00000177694.1:p.Arg34=
ENST00000581328.1:n.132C>T
NM_013351.1:c.102C>T NP_037483.1:p.Arg34=
XM_011524698.1:c.102C>T XP_011523000.1:p.Arg34=
NM_013351.2:c.102C>T MANE Select NP_037483.1:p.Arg34=
Search 100 bp 5'
Search 100 bp 3'