Canonical Allele Identifier: CA1205614072
Gene: TBX19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293024_168293026delinsATG , CM000663.2:g.168293024_168293026delinsATG GRCh38
NC_000001.10:g.168262262_168262264delinsATG , CM000663.1:g.168262262_168262264delinsATG GRCh37
NC_000001.9:g.166528886_166528888delinsATG NCBI36
NG_008244.1:g.16985_16987delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.469-120_469-118delinsATG MANE Select ENSP00000356795.3:n.469-120_469-118delinsATG
ENST00000367821.7:c.469-120_469-118delinsATG ENSP00000356795.3:n.469-120_469-118delinsATG
ENST00000431969.5:c.266-120_266-118delinsATG
NM_005149.2:c.469-120_469-118delinsATG NP_005140.1:n.469-120_469-118delinsATG
NM_005149.3:c.469-120_469-118delinsATG MANE Select NP_005140.1:n.469-120_469-118delinsATG
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