Canonical Allele Identifier: CA2636259643

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999817-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999817G>T , CM000679.2:g.15999817G>T	GRCh38
NC_000017.10:g.15903131G>T , CM000679.1:g.15903131G>T	GRCh37
NC_000017.9:g.15843856G>T	NCBI36
NG_029806.1:g.5438G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-32G>T	ENSP00000261647.5:n.-32G>T
ENST00000466729.5:c.34G>T
ENST00000475723.5:c.16G>T
NM_001271420.1:c.-490G>T	NP_001258349.1:n.-490G>T
NM_017775.3:c.-32G>T	NP_060245.3:n.-32G>T
XM_011523950.1:c.-32G>T	XP_011522252.1:n.-32G>T
XM_017024801.2:c.-32G>T	XP_016880290.2:n.-32G>T
XM_017024802.2:c.-32G>T	XP_016880291.2:n.-32G>T
XM_024450814.1:c.-32G>T	XP_024306582.1:n.-32G>T