Canonical Allele Identifier: CA2739521120
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999735C>G , CM000679.2:g.15999735C>G GRCh38
NC_000017.10:g.15903049C>G , CM000679.1:g.15903049C>G GRCh37
NC_000017.9:g.15843774C>G NCBI36
NG_029806.1:g.5356C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-114C>G ENSP00000261647.5:n.-114C>G
NM_001271420.1:c.-572C>G NP_001258349.1:n.-572C>G
NM_017775.3:c.-114C>G NP_060245.3:n.-114C>G