Canonical Allele Identifier: CA2649007554
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293321_168293323dup , CM000663.2:g.168293321_168293323dup GRCh38
NC_000001.10:g.168262559_168262561dup , CM000663.1:g.168262559_168262561dup GRCh37
NC_000001.9:g.166529183_166529185dup NCBI36
NG_008244.1:g.17282_17284dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+43_603+45dup MANE Select ENSP00000356795.3:n.603+43_603+45dup
ENST00000367821.7:c.603+43_603+45dup ENSP00000356795.3:n.603+43_603+45dup
ENST00000431969.5:c.400+43_400+45dup
NM_005149.2:c.603+43_603+45dup NP_005140.1:n.603+43_603+45dup
NM_005149.3:c.603+43_603+45dup MANE Select NP_005140.1:n.603+43_603+45dup