Canonical Allele Identifier: CA2249814903
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999801G= , CM000679.2:g.15999801G= GRCh38
NC_000017.10:g.15903115G= , CM000679.1:g.15903115G= GRCh37
NC_000017.9:g.15843840G= NCBI36
NG_029806.1:g.5422G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-48G= ENSP00000261647.5:n.-48G=
ENST00000466729.5:c.18G=
NM_001271420.1:c.-506G= NP_001258349.1:n.-506G=
NM_017775.3:c.-48G= NP_060245.3:n.-48G=
XM_011523950.1:c.-48G= XP_011522252.1:n.-48G=
XM_017024801.2:c.-48G= XP_016880290.2:n.-48G=
XM_017024802.2:c.-48G= XP_016880291.2:n.-48G=
XM_024450814.1:c.-48G= XP_024306582.1:n.-48G=