Canonical Allele Identifier: CA2249814865
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999757G= , CM000679.2:g.15999757G= GRCh38
NC_000017.10:g.15903071G= , CM000679.1:g.15903071G= GRCh37
NC_000017.9:g.15843796G= NCBI36
NG_029806.1:g.5378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-92G= ENSP00000261647.5:n.-92G=
NM_001271420.1:c.-550G= NP_001258349.1:n.-550G=
NM_017775.3:c.-92G= NP_060245.3:n.-92G=
XM_011523950.1:c.-92G= XP_011522252.1:n.-92G=