Canonical Allele Identifier: CA2649007461
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168293056-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293056T>A , CM000663.2:g.168293056T>A GRCh38
NC_000001.10:g.168262294T>A , CM000663.1:g.168262294T>A GRCh37
NC_000001.9:g.166528918T>A NCBI36
NG_008244.1:g.17017T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.469-88T>A MANE Select ENSP00000356795.3:n.469-88T>A
ENST00000367821.7:c.469-88T>A ENSP00000356795.3:n.469-88T>A
ENST00000431969.5:c.266-88T>A
NM_005149.2:c.469-88T>A NP_005140.1:n.469-88T>A
NM_005149.3:c.469-88T>A MANE Select NP_005140.1:n.469-88T>A
Search 100 bp 5'
Search 100 bp 3'