Canonical Allele Identifier: CA1205614176
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs1648994401
gnomAD v4: 1-168293284-A-AGAGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293285_168293286insAGTG , CM000663.2:g.168293285_168293286insAGTG GRCh38
NC_000001.10:g.168262523_168262524insAGTG , CM000663.1:g.168262523_168262524insAGTG GRCh37
NC_000001.9:g.166529147_166529148insAGTG NCBI36
NG_008244.1:g.17246_17247insAGTG

Transcript Alleles

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