Canonical Allele Identifier: CA820813823

Gene: CCDC170

Linked Data

• dbSNP Id: rs1355199635
• gnomAD v3: 6-151526776-G-C
• gnomAD v4: 6-151526776-G-C
• MyVariant Identifiers: chr6:g.151847911G>C (hg19) ; chr6:g.151526776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151526776G>C , CM000668.2:g.151526776G>C	GRCh38
NC_000006.11:g.151847911G>C , CM000668.1:g.151847911G>C	GRCh37
NC_000006.10:g.151889604G>C	NCBI36
NG_021198.1:g.37737G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.58-9542G>C MANE Select	ENSP00000239374.6:n.58-9542G>C
ENST00000239374.7:c.58-9542G>C	ENSP00000239374.6:n.58-9542G>C
NM_025059.3:c.58-9542G>C	NP_079335.2:n.58-9542G>C
NM_025059.4:c.58-9542G>C MANE Select	NP_079335.2:n.58-9542G>C