Canonical Allele Identifier: CA2249814870
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999764C= , CM000679.2:g.15999764C= GRCh38
NC_000017.10:g.15903078C= , CM000679.1:g.15903078C= GRCh37
NC_000017.9:g.15843803C= NCBI36
NG_029806.1:g.5385C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-85C= ENSP00000261647.5:n.-85C=
NM_001271420.1:c.-543C= NP_001258349.1:n.-543C=
NM_017775.3:c.-85C= NP_060245.3:n.-85C=
XM_011523950.1:c.-85C= XP_011522252.1:n.-85C=