Canonical Allele Identifier: CA2576180949

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999800-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999800G>T , CM000679.2:g.15999800G>T	GRCh38
NC_000017.10:g.15903114G>T , CM000679.1:g.15903114G>T	GRCh37
NC_000017.9:g.15843839G>T	NCBI36
NG_029806.1:g.5421G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-49G>T	ENSP00000261647.5:n.-49G>T
ENST00000466729.5:c.17G>T
NM_001271420.1:c.-507G>T	NP_001258349.1:n.-507G>T
NM_017775.3:c.-49G>T	NP_060245.3:n.-49G>T
XM_011523950.1:c.-49G>T	XP_011522252.1:n.-49G>T
XM_017024801.2:c.-49G>T	XP_016880290.2:n.-49G>T
XM_017024802.2:c.-49G>T	XP_016880291.2:n.-49G>T
XM_024450814.1:c.-49G>T	XP_024306582.1:n.-49G>T