Canonical Allele Identifier: CA2636259522
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999724G>T , CM000679.2:g.15999724G>T GRCh38
NC_000017.10:g.15903038G>T , CM000679.1:g.15903038G>T GRCh37
NC_000017.9:g.15843763G>T NCBI36
NG_029806.1:g.5345G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-125G>T ENSP00000261647.5:n.-125G>T
NM_001271420.1:c.-583G>T NP_001258349.1:n.-583G>T
NM_017775.3:c.-125G>T NP_060245.3:n.-125G>T