Canonical Allele Identifier: CA1230523
Gene: TBX19 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 293458
ClinVar RCV Id: RCV000406538
dbSNP Id: rs200197424

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293210C>T , CM000663.2:g.168293210C>T GRCh38
NC_000001.9:g.166529072C>T NCBI36
NC_000001.10:g.168262448C>T , CM000663.1:g.168262448C>T GRCh37
NG_008244.1:g.17171C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.7:c.535C>T ENSP00000356795.3:p.Arg179Ter
ENST00000431969.5:n.332C>T
NM_005149.2:c.535C>T VV NP_005140.1:p.Arg179Ter