Canonical Allele Identifier: CA2739521138

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999768G>C , CM000679.2:g.15999768G>C	GRCh38
NC_000017.10:g.15903082G>C , CM000679.1:g.15903082G>C	GRCh37
NC_000017.9:g.15843807G>C	NCBI36
NG_029806.1:g.5389G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-81G>C	ENSP00000261647.5:n.-81G>C
NM_001271420.1:c.-539G>C	NP_001258349.1:n.-539G>C
NM_017775.3:c.-81G>C	NP_060245.3:n.-81G>C
XM_011523950.1:c.-81G>C	XP_011522252.1:n.-81G>C