Canonical Allele Identifier: CA1205614241
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs1649001853

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293358dup , CM000663.2:g.168293358dup GRCh38
NC_000001.10:g.168262596dup , CM000663.1:g.168262596dup GRCh37
NC_000001.9:g.166529220dup NCBI36
NG_008244.1:g.17319dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+80dup MANE Select ENSP00000356795.3:n.603+80dup
ENST00000367821.7:c.603+80dup ENSP00000356795.3:n.603+80dup
ENST00000431969.5:c.400+80dup
NM_005149.2:c.603+80dup NP_005140.1:n.603+80dup
NM_005149.3:c.603+80dup MANE Select NP_005140.1:n.603+80dup