Canonical Allele Identifier: CA1205614131
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293162C= , CM000663.2:g.168293162C= GRCh38
NC_000001.10:g.168262400C= , CM000663.1:g.168262400C= GRCh37
NC_000001.9:g.166529024C= NCBI36
NG_008244.1:g.17123C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.487C= MANE Select ENSP00000356795.3:p.His163=
ENST00000367821.7:c.487C= ENSP00000356795.3:p.His163=
ENST00000431969.5:c.284C=
NM_005149.2:c.487C= NP_005140.1:p.His163=
NM_005149.3:c.487C= MANE Select NP_005140.1:p.His163=
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