Canonical Allele Identifier: CA1205614085
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293043G= , CM000663.2:g.168293043G= GRCh38
NC_000001.10:g.168262281G= , CM000663.1:g.168262281G= GRCh37
NC_000001.9:g.166528905G= NCBI36
NG_008244.1:g.17004G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-101G= MANE Select ENSP00000356795.3:n.469-101G=
ENST00000367821.7:c.469-101G= ENSP00000356795.3:n.469-101G=
ENST00000431969.5:c.266-101G=
NM_005149.2:c.469-101G= NP_005140.1:n.469-101G=
NM_005149.3:c.469-101G= MANE Select NP_005140.1:n.469-101G=
Search 100 bp 5'
Search 100 bp 3'