Canonical Allele Identifier: CA291430

Gene: TTC19

Linked Data

• ClinVar Variation Id: 137771
• ClinVar RCV Id: RCV000125732 ; RCV000359020
• dbSNP Id: rs79724115
• ExAC: 17:15903056 A / T
• gnomAD v2: 17-15903056-A-T
• gnomAD v3: 17-15999742-A-T
• gnomAD v4: 17-15999742-A-T
• MyVariant Identifiers: chr17:g.15903056A>T (hg19) ; chr17:g.15999742A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999742A>T , CM000679.2:g.15999742A>T	GRCh38
NC_000017.10:g.15903056A>T , CM000679.1:g.15903056A>T	GRCh37
NC_000017.9:g.15843781A>T	NCBI36
NG_029806.1:g.5363A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.9:c.-107A>T	ENSP00000261647.5:n.-107A>T
NM_001271420.1:c.-565A>T	NP_001258349.1:n.-565A>T
NM_017775.3:c.-107A>T	NP_060245.3:n.-107A>T