Canonical Allele Identifier: CA1672929518

Gene: CCDC170

Linked Data

• dbSNP Id: rs1782415416

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151526643G>A , CM000668.2:g.151526643G>A	GRCh38
NC_000006.11:g.151847778G>A , CM000668.1:g.151847778G>A	GRCh37
NC_000006.10:g.151889471G>A	NCBI36
NG_021198.1:g.37604G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.58-9675G>A MANE Select	ENSP00000239374.6:n.58-9675G>A
ENST00000239374.7:c.58-9675G>A	ENSP00000239374.6:n.58-9675G>A
NM_025059.3:c.58-9675G>A	NP_079335.2:n.58-9675G>A
NM_025059.4:c.58-9675G>A MANE Select	NP_079335.2:n.58-9675G>A