Canonical Allele Identifier: CA1205614304
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293478_168293479delinsAC , CM000663.2:g.168293478_168293479delinsAC GRCh38
NC_000001.10:g.168262716_168262717delinsAC , CM000663.1:g.168262716_168262717delinsAC GRCh37
NC_000001.9:g.166529340_166529341delinsAC NCBI36
NG_008244.1:g.17439_17440delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+200_603+201delinsAC MANE Select ENSP00000356795.3:n.603+200_603+201delinsAC
ENST00000367821.7:c.603+200_603+201delinsAC ENSP00000356795.3:n.603+200_603+201delinsAC
ENST00000431969.5:c.400+200_400+201delinsAC
NM_005149.2:c.603+200_603+201delinsAC NP_005140.1:n.603+200_603+201delinsAC
NM_005149.3:c.603+200_603+201delinsAC MANE Select NP_005140.1:n.603+200_603+201delinsAC