Canonical Allele Identifier: CA2249814856
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999747C= , CM000679.2:g.15999747C= GRCh38
NC_000017.10:g.15903061C= , CM000679.1:g.15903061C= GRCh37
NC_000017.9:g.15843786C= NCBI36
NG_029806.1:g.5368C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-102C= ENSP00000261647.5:n.-102C=
NM_001271420.1:c.-560C= NP_001258349.1:n.-560C=
NM_017775.3:c.-102C= NP_060245.3:n.-102C=