Canonical Allele Identifier: CA1205614067
Gene: TBX19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293012C= , CM000663.2:g.168293012C= GRCh38
NC_000001.10:g.168262250C= , CM000663.1:g.168262250C= GRCh37
NC_000001.9:g.166528874C= NCBI36
NG_008244.1:g.16973C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-132C= MANE Select ENSP00000356795.3:n.469-132C=
ENST00000367821.7:c.469-132C= ENSP00000356795.3:n.469-132C=
ENST00000431969.5:c.266-132C=
NM_005149.2:c.469-132C= NP_005140.1:n.469-132C=
NM_005149.3:c.469-132C= MANE Select NP_005140.1:n.469-132C=
Search 100 bp 5'
Search 100 bp 3'