Canonical Allele Identifier: CA8407225

Gene: TTC19

Linked Data

• dbSNP Id: rs773326202
• ExAC: 17:15903136 G / A
• gnomAD v2: 17-15903136-G-A
• gnomAD v4: 17-15999822-G-A
• MyVariant Identifiers: chr17:g.15903136G>A (hg19) ; chr17:g.15999822G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999822G>A , CM000679.2:g.15999822G>A	GRCh38
NC_000017.10:g.15903136G>A , CM000679.1:g.15903136G>A	GRCh37
NC_000017.9:g.15843861G>A	NCBI36
NG_029806.1:g.5443G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-27G>A	ENSP00000261647.5:n.-27G>A
ENST00000466729.5:c.39G>A
ENST00000475723.5:c.21G>A
NM_001271420.1:c.-485G>A	NP_001258349.1:n.-485G>A
NM_017775.3:c.-27G>A	NP_060245.3:n.-27G>A
XM_011523950.1:c.-27G>A	XP_011522252.1:n.-27G>A
XM_017024801.2:c.-27G>A	XP_016880290.2:n.-27G>A
XM_017024802.2:c.-27G>A	XP_016880291.2:n.-27G>A
XM_024450814.1:c.-27G>A	XP_024306582.1:n.-27G>A