Canonical Allele Identifier: CA1205613293
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291139A= , CM000663.2:g.168291139A= GRCh38
NC_000001.10:g.168260377A= , CM000663.1:g.168260377A= GRCh37
NC_000001.9:g.166527001A= NCBI36
NG_008244.1:g.15100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-21A= MANE Select ENSP00000356795.3:n.204-21A=
ENST00000367821.7:c.204-21A= ENSP00000356795.3:n.204-21A=
NM_005149.2:c.204-21A= NP_005140.1:n.204-21A=
NM_005149.3:c.204-21A= MANE Select NP_005140.1:n.204-21A=
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