Canonical Allele Identifier: CA343107047
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293240A>T , CM000663.2:g.168293240A>T GRCh38
NC_000001.10:g.168262478A>T , CM000663.1:g.168262478A>T GRCh37
NC_000001.9:g.166529102A>T NCBI36
NG_008244.1:g.17201A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.565A>T MANE Select ENSP00000356795.3:p.Thr189Ser
ENST00000367821.7:c.565A>T ENSP00000356795.3:p.Thr189Ser
ENST00000431969.5:c.362A>T
NM_005149.2:c.565A>T NP_005140.1:p.Thr189Ser
NM_005149.3:c.565A>T MANE Select NP_005140.1:p.Thr189Ser