Canonical Allele Identifier: CA1205614235
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293347T= , CM000663.2:g.168293347T= GRCh38
NC_000001.10:g.168262585T= , CM000663.1:g.168262585T= GRCh37
NC_000001.9:g.166529209T= NCBI36
NG_008244.1:g.17308T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+69T= MANE Select ENSP00000356795.3:n.603+69T=
ENST00000367821.7:c.603+69T= ENSP00000356795.3:n.603+69T=
ENST00000431969.5:c.400+69T=
NM_005149.2:c.603+69T= NP_005140.1:n.603+69T=
NM_005149.3:c.603+69T= MANE Select NP_005140.1:n.603+69T=