Canonical Allele Identifier: CA343107000
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293220C>G , CM000663.2:g.168293220C>G GRCh38
NC_000001.10:g.168262458C>G , CM000663.1:g.168262458C>G GRCh37
NC_000001.9:g.166529082C>G NCBI36
NG_008244.1:g.17181C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.545C>G MANE Select ENSP00000356795.3:p.Thr182Arg
ENST00000367821.7:c.545C>G ENSP00000356795.3:p.Thr182Arg
ENST00000431969.5:c.342C>G
NM_005149.2:c.545C>G NP_005140.1:p.Thr182Arg
NM_005149.3:c.545C>G MANE Select NP_005140.1:p.Thr182Arg