Canonical Allele Identifier: CA343106995
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293217T>A , CM000663.2:g.168293217T>A GRCh38
NC_000001.10:g.168262455T>A , CM000663.1:g.168262455T>A GRCh37
NC_000001.9:g.166529079T>A NCBI36
NG_008244.1:g.17178T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.542T>A MANE Select ENSP00000356795.3:p.Val181Glu
ENST00000367821.7:c.542T>A ENSP00000356795.3:p.Val181Glu
ENST00000431969.5:c.339T>A
NM_005149.2:c.542T>A NP_005140.1:p.Val181Glu
NM_005149.3:c.542T>A MANE Select NP_005140.1:p.Val181Glu