Canonical Allele Identifier: CA2249814834
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999721A= , CM000679.2:g.15999721A= GRCh38
NC_000017.10:g.15903035A= , CM000679.1:g.15903035A= GRCh37
NC_000017.9:g.15843760A= NCBI36
NG_029806.1:g.5342A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-128A= ENSP00000261647.5:n.-128A=
NM_001271420.1:c.-586A= NP_001258349.1:n.-586A=
NM_017775.3:c.-128A= NP_060245.3:n.-128A=