Canonical Allele Identifier: CA1205614098
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293063A= , CM000663.2:g.168293063A= GRCh38
NC_000001.10:g.168262301A= , CM000663.1:g.168262301A= GRCh37
NC_000001.9:g.166528925A= NCBI36
NG_008244.1:g.17024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-81A= MANE Select ENSP00000356795.3:n.469-81A=
ENST00000367821.7:c.469-81A= ENSP00000356795.3:n.469-81A=
ENST00000431969.5:c.266-81A=
NM_005149.2:c.469-81A= NP_005140.1:n.469-81A=
NM_005149.3:c.469-81A= MANE Select NP_005140.1:n.469-81A=
Search 100 bp 5'
Search 100 bp 3'