Canonical Allele Identifier: CA2649007559
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293327_168293328dup , CM000663.2:g.168293327_168293328dup GRCh38
NC_000001.10:g.168262565_168262566dup , CM000663.1:g.168262565_168262566dup GRCh37
NC_000001.9:g.166529189_166529190dup NCBI36
NG_008244.1:g.17288_17289dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+49_603+50dup MANE Select ENSP00000356795.3:n.603+49_603+50dup
ENST00000367821.7:c.603+49_603+50dup ENSP00000356795.3:n.603+49_603+50dup
ENST00000431969.5:c.400+49_400+50dup
NM_005149.2:c.603+49_603+50dup NP_005140.1:n.603+49_603+50dup
NM_005149.3:c.603+49_603+50dup MANE Select NP_005140.1:n.603+49_603+50dup