Canonical Allele Identifier: CA2636259547
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-15999746-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999746C>A , CM000679.2:g.15999746C>A GRCh38
NC_000017.10:g.15903060C>A , CM000679.1:g.15903060C>A GRCh37
NC_000017.9:g.15843785C>A NCBI36
NG_029806.1:g.5367C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-103C>A ENSP00000261647.5:n.-103C>A
NM_001271420.1:c.-561C>A NP_001258349.1:n.-561C>A
NM_017775.3:c.-103C>A NP_060245.3:n.-103C>A
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