Canonical Allele Identifier: CA343105770
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291217C>A , CM000663.2:g.168291217C>A GRCh38
NC_000001.10:g.168260455C>A , CM000663.1:g.168260455C>A GRCh37
NC_000001.9:g.166527079C>A NCBI36
NG_008244.1:g.15178C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.261C>A MANE Select ENSP00000356795.3:p.Tyr87Ter
ENST00000367821.7:c.261C>A ENSP00000356795.3:p.Tyr87Ter
ENST00000431969.5:c.58C>A
NM_005149.2:c.261C>A NP_005140.1:p.Tyr87Ter
NM_005149.3:c.261C>A MANE Select NP_005140.1:p.Tyr87Ter