Canonical Allele Identifier: CA624961131
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1419606629
gnomAD v2: 17-15903062-T-C
gnomAD v4: 17-15999748-T-C
MyVariant Identifiers: chr17:g.15903062T>C (hg19) chr17:g.15999748T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999748T>C , CM000679.2:g.15999748T>C GRCh38
NC_000017.10:g.15903062T>C , CM000679.1:g.15903062T>C GRCh37
NC_000017.9:g.15843787T>C NCBI36
NG_029806.1:g.5369T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-101T>C ENSP00000261647.5:n.-101T>C
NM_001271420.1:c.-559T>C NP_001258349.1:n.-559T>C
NM_017775.3:c.-101T>C NP_060245.3:n.-101T>C
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