Canonical Allele Identifier: CA1143975114
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291122C= , CM000663.2:g.168291122C= GRCh38
NC_000001.10:g.168260360C= , CM000663.1:g.168260360C= GRCh37
NC_000001.9:g.166526984C= NCBI36
NG_008244.1:g.15083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-38C= MANE Select ENSP00000356795.3:n.204-38C=
ENST00000367821.7:c.204-38C= ENSP00000356795.3:n.204-38C=
NM_005149.2:c.204-38C= NP_005140.1:n.204-38C=
NM_005149.3:c.204-38C= MANE Select NP_005140.1:n.204-38C=