Canonical Allele Identifier: CA2739521116

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999730G>C , CM000679.2:g.15999730G>C	GRCh38
NC_000017.10:g.15903044G>C , CM000679.1:g.15903044G>C	GRCh37
NC_000017.9:g.15843769G>C	NCBI36
NG_029806.1:g.5351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-119G>C	ENSP00000261647.5:n.-119G>C
NM_001271420.1:c.-577G>C	NP_001258349.1:n.-577G>C
NM_017775.3:c.-119G>C	NP_060245.3:n.-119G>C