Canonical Allele Identifier: CA343107039
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293237G>C , CM000663.2:g.168293237G>C GRCh38
NC_000001.10:g.168262475G>C , CM000663.1:g.168262475G>C GRCh37
NC_000001.9:g.166529099G>C NCBI36
NG_008244.1:g.17198G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.562G>C MANE Select ENSP00000356795.3:p.Glu188Gln
ENST00000367821.7:c.562G>C ENSP00000356795.3:p.Glu188Gln
ENST00000431969.5:c.359G>C
NM_005149.2:c.562G>C NP_005140.1:p.Glu188Gln
NM_005149.3:c.562G>C MANE Select NP_005140.1:p.Glu188Gln