Canonical Allele Identifier: CA2739521128
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999743T>G , CM000679.2:g.15999743T>G GRCh38
NC_000017.10:g.15903057T>G , CM000679.1:g.15903057T>G GRCh37
NC_000017.9:g.15843782T>G NCBI36
NG_029806.1:g.5364T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-106T>G ENSP00000261647.5:n.-106T>G
NM_001271420.1:c.-564T>G NP_001258349.1:n.-564T>G
NM_017775.3:c.-106T>G NP_060245.3:n.-106T>G