Canonical Allele Identifier: CA624961140

Gene: TTC19

Linked Data

• dbSNP Id: rs1293661722
• gnomAD v2: 17-15903089-C-T
• gnomAD v4: 17-15999775-C-T
• MyVariant Identifiers: chr17:g.15903089C>T (hg19) ; chr17:g.15999775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999775C>T , CM000679.2:g.15999775C>T	GRCh38
NC_000017.10:g.15903089C>T , CM000679.1:g.15903089C>T	GRCh37
NC_000017.9:g.15843814C>T	NCBI36
NG_029806.1:g.5396C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-74C>T	ENSP00000261647.5:n.-74C>T
NM_001271420.1:c.-532C>T	NP_001258349.1:n.-532C>T
NM_017775.3:c.-74C>T	NP_060245.3:n.-74C>T
XM_011523950.1:c.-74C>T	XP_011522252.1:n.-74C>T
XM_017024801.2:c.-74C>T	XP_016880290.2:n.-74C>T
XM_017024802.2:c.-74C>T	XP_016880291.2:n.-74C>T
XM_024450814.1:c.-74C>T	XP_024306582.1:n.-74C>T