Canonical Allele Identifier: CA1008886821
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs1649002792
gnomAD v3: 1-168293363-G-GT
gnomAD v4: 1-168293363-G-GT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293363_168293364insT , CM000663.2:g.168293363_168293364insT GRCh38
NC_000001.10:g.168262601_168262602insT , CM000663.1:g.168262601_168262602insT GRCh37
NC_000001.9:g.166529225_166529226insT NCBI36
NG_008244.1:g.17324_17325insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+85_603+86insT MANE Select ENSP00000356795.3:n.603+85_603+86insT
ENST00000367821.7:c.603+85_603+86insT ENSP00000356795.3:n.603+85_603+86insT
ENST00000431969.5:c.400+85_400+86insT
NM_005149.2:c.603+85_603+86insT NP_005140.1:n.603+85_603+86insT
NM_005149.3:c.603+85_603+86insT MANE Select NP_005140.1:n.603+85_603+86insT
Search 100 bp 5'
Search 100 bp 3'