Canonical Allele Identifier: CA2249814862
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999754G= , CM000679.2:g.15999754G= GRCh38
NC_000017.10:g.15903068G= , CM000679.1:g.15903068G= GRCh37
NC_000017.9:g.15843793G= NCBI36
NG_029806.1:g.5375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-95G= ENSP00000261647.5:n.-95G=
NM_001271420.1:c.-553G= NP_001258349.1:n.-553G=
NM_017775.3:c.-95G= NP_060245.3:n.-95G=
XM_011523950.1:c.-95G= XP_011522252.1:n.-95G=