Canonical Allele Identifier: CA1008886756
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v3: 1-168293326-T-TGTGTG
gnomAD v4: 1-168293326-T-TGTGTG
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293326_168293327insGTGTG , CM000663.2:g.168293326_168293327insGTGTG GRCh38
NC_000001.10:g.168262564_168262565insGTGTG , CM000663.1:g.168262564_168262565insGTGTG GRCh37
NC_000001.9:g.166529188_166529189insGTGTG NCBI36
NG_008244.1:g.17287_17288insGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+48_603+49insGTGTG MANE Select ENSP00000356795.3:n.603+48_603+49insGTGTG
ENST00000367821.7:c.603+48_603+49insGTGTG ENSP00000356795.3:n.603+48_603+49insGTGTG
ENST00000431969.5:c.400+48_400+49insGTGTG
NM_005149.2:c.603+48_603+49insGTGTG NP_005140.1:n.603+48_603+49insGTGTG
NM_005149.3:c.603+48_603+49insGTGTG MANE Select NP_005140.1:n.603+48_603+49insGTGTG
Search 100 bp 5'
Search 100 bp 3'