Canonical Allele Identifier: CA1205613292
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291133T= , CM000663.2:g.168291133T= GRCh38
NC_000001.10:g.168260371T= , CM000663.1:g.168260371T= GRCh37
NC_000001.9:g.166526995T= NCBI36
NG_008244.1:g.15094T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-27T= MANE Select ENSP00000356795.3:n.204-27T=
ENST00000367821.7:c.204-27T= ENSP00000356795.3:n.204-27T=
NM_005149.2:c.204-27T= NP_005140.1:n.204-27T=
NM_005149.3:c.204-27T= MANE Select NP_005140.1:n.204-27T=
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