Canonical Allele Identifier: CA8626429
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs191857237
ExAC: 17:45822102 A / G
gnomAD v2: 17-45822102-A-G
gnomAD v3: 17-47744736-A-G
gnomAD v4: 17-47744736-A-G
MyVariant Identifiers: chr17:g.45822102A>G (hg19) chr17:g.47744736A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47744736A>G , CM000679.2:g.47744736A>G GRCh38
NC_000017.10:g.45822102A>G , CM000679.1:g.45822102A>G GRCh37
NC_000017.9:g.43177101A>G NCBI36
NG_012166.1:g.16493A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.990-12A>G MANE Select ENSP00000177694.1:n.990-12A>G
ENST00000177694.1:c.990-12A>G ENSP00000177694.1:n.990-12A>G
NM_013351.1:c.990-12A>G NP_037483.1:n.990-12A>G
XM_011524698.1:c.1053-12A>G XP_011523000.1:n.1053-12A>G
XM_011524699.1:c.657-12A>G XP_011523001.1:n.657-12A>G
NM_013351.2:c.990-12A>G MANE Select NP_037483.1:n.990-12A>G
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