Canonical Allele Identifier: CA2249814844
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999728G= , CM000679.2:g.15999728G= GRCh38
NC_000017.10:g.15903042G= , CM000679.1:g.15903042G= GRCh37
NC_000017.9:g.15843767G= NCBI36
NG_029806.1:g.5349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-121G= ENSP00000261647.5:n.-121G=
NM_001271420.1:c.-579G= NP_001258349.1:n.-579G=
NM_017775.3:c.-121G= NP_060245.3:n.-121G=