Canonical Allele Identifier: CA500652449
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs2032168047
gnomAD v4: 17-47733658-G-A
MyVariant Identifiers: chr17:g.45811024G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733658G>A , CM000679.2:g.47733658G>A GRCh38
NC_000017.10:g.45811024G>A , CM000679.1:g.45811024G>A GRCh37
NC_000017.9:g.43166023G>A NCBI36
NG_012166.1:g.5415G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.204G>A MANE Select ENSP00000177694.1:p.Pro68=
ENST00000177694.1:c.204G>A ENSP00000177694.1:p.Pro68=
ENST00000581328.1:n.234G>A
NM_013351.1:c.204G>A NP_037483.1:p.Pro68=
XM_011524698.1:c.204G>A XP_011523000.1:p.Pro68=
NM_013351.2:c.204G>A MANE Select NP_037483.1:p.Pro68=
Search 100 bp 5'
Search 100 bp 3'