Canonical Allele Identifier: CA2636259578
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-15999768-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999768G>A , CM000679.2:g.15999768G>A GRCh38
NC_000017.10:g.15903082G>A , CM000679.1:g.15903082G>A GRCh37
NC_000017.9:g.15843807G>A NCBI36
NG_029806.1:g.5389G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-81G>A ENSP00000261647.5:n.-81G>A
NM_001271420.1:c.-539G>A NP_001258349.1:n.-539G>A
NM_017775.3:c.-81G>A NP_060245.3:n.-81G>A
XM_011523950.1:c.-81G>A XP_011522252.1:n.-81G>A
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