Canonical Allele Identifier: CA500652446
Gene: TBX21 HGNC NCBI

Linked Data

gnomAD v4: 17-47733856-G-A
MyVariant Identifiers: chr17:g.45811222G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733856G>A , CM000679.2:g.47733856G>A GRCh38
NC_000017.10:g.45811222G>A , CM000679.1:g.45811222G>A GRCh37
NC_000017.9:g.43166221G>A NCBI36
NG_012166.1:g.5613G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.402G>A MANE Select ENSP00000177694.1:p.Ser134=
ENST00000177694.1:c.402G>A ENSP00000177694.1:p.Ser134=
ENST00000581328.1:n.432G>A
NM_013351.1:c.402G>A NP_037483.1:p.Ser134=
XM_011524698.1:c.402G>A XP_011523000.1:p.Ser134=
NM_013351.2:c.402G>A MANE Select NP_037483.1:p.Ser134=
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