Canonical Allele Identifier: CA2249814872
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999766C= , CM000679.2:g.15999766C= GRCh38
NC_000017.10:g.15903080C= , CM000679.1:g.15903080C= GRCh37
NC_000017.9:g.15843805C= NCBI36
NG_029806.1:g.5387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-83C= ENSP00000261647.5:n.-83C=
NM_001271420.1:c.-541C= NP_001258349.1:n.-541C=
NM_017775.3:c.-83C= NP_060245.3:n.-83C=
XM_011523950.1:c.-83C= XP_011522252.1:n.-83C=