Canonical Allele Identifier: CA1143601663
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291123G= , CM000663.2:g.168291123G= GRCh38
NC_000001.10:g.168260361G= , CM000663.1:g.168260361G= GRCh37
NC_000001.9:g.166526985G= NCBI36
NG_008244.1:g.15084G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-37G= MANE Select ENSP00000356795.3:n.204-37G=
ENST00000367821.7:c.204-37G= ENSP00000356795.3:n.204-37G=
NM_005149.2:c.204-37G= NP_005140.1:n.204-37G=
NM_005149.3:c.204-37G= MANE Select NP_005140.1:n.204-37G=
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