Canonical Allele Identifier: CA2649007495
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168293110-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293114dup , CM000663.2:g.168293114dup GRCh38
NC_000001.10:g.168262352dup , CM000663.1:g.168262352dup GRCh37
NC_000001.9:g.166528976dup NCBI36
NG_008244.1:g.17075dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-30dup MANE Select ENSP00000356795.3:n.469-30dup
ENST00000367821.7:c.469-30dup ENSP00000356795.3:n.469-30dup
ENST00000431969.5:c.266-30dup
NM_005149.2:c.469-30dup NP_005140.1:n.469-30dup
NM_005149.3:c.469-30dup MANE Select NP_005140.1:n.469-30dup
Search 100 bp 5'
Search 100 bp 3'