Canonical Allele Identifier: CA343105805
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291222T>G , CM000663.2:g.168291222T>G GRCh38
NC_000001.10:g.168260460T>G , CM000663.1:g.168260460T>G GRCh37
NC_000001.9:g.166527084T>G NCBI36
NG_008244.1:g.15183T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.266T>G MANE Select ENSP00000356795.3:p.Leu89Arg
ENST00000367821.7:c.266T>G ENSP00000356795.3:p.Leu89Arg
ENST00000431969.5:c.63T>G
NM_005149.2:c.266T>G NP_005140.1:p.Leu89Arg
NM_005149.3:c.266T>G MANE Select NP_005140.1:p.Leu89Arg