Canonical Allele Identifier: CA981831980
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1971666098
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028502T>A , CM000679.2:g.16028502T>A GRCh38
NC_000017.10:g.15931816T>A , CM000679.1:g.15931816T>A GRCh37
NC_000017.9:g.15872541T>A NCBI36
NG_029806.1:g.34123T>A
NG_047111.1:g.193245A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*980T>A MANE Select ENSP00000261647.5:n.*980T>A
ENST00000261647.9:c.*980T>A ENSP00000261647.5:n.*980T>A
ENST00000465567.1:n.2517T>A
ENST00000470649.1:c.247+1800T>A ENSP00000465627.1:n.247+1800T>A
ENST00000475723.5:c.2307T>A
ENST00000481107.1:n.2791T>A
NM_001271420.1:c.*980T>A NP_001258349.1:n.*980T>A
NM_017775.3:c.*980T>A NP_060245.3:n.*980T>A
XM_017024801.2:c.994+1800T>A XP_016880290.2:n.994+1800T>A
XM_017024802.2:c.994+1800T>A XP_016880291.2:n.994+1800T>A
NM_017775.4:c.*980T>A MANE Select NP_060245.3:n.*980T>A
NM_001271420.2:c.*980T>A NP_001258349.1:n.*980T>A
Search 100 bp 5'
Search 100 bp 3'