Canonical Allele Identifier: CA2636259519
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-15999721-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999721A>T , CM000679.2:g.15999721A>T GRCh38
NC_000017.10:g.15903035A>T , CM000679.1:g.15903035A>T GRCh37
NC_000017.9:g.15843760A>T NCBI36
NG_029806.1:g.5342A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-128A>T ENSP00000261647.5:n.-128A>T
NM_001271420.1:c.-586A>T NP_001258349.1:n.-586A>T
NM_017775.3:c.-128A>T NP_060245.3:n.-128A>T
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