Canonical Allele Identifier: CA150138001
Gene: CCDC170 HGNC NCBI
COSMIC:
COSN14772700 (not active)
MyVariant.info:
GRCh38 chr6:g.151526832C>A
GRCh37 chr6:g.151847967C>A
gnomAD v2:
6:151847967 C / A
gnomAD v3:
6:151526832 C / A
gnomAD v4:
chr6-151526832-C-A
Joint Max Group AF 0.5974919 (NFE)
Genomes Max Group AF 0.5974919 (NFE)
dbSNP:
9479055
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526832C>A , CM000668.2:g.151526832C>A GRCh38
NC_000006.11:g.151847967C>A , CM000668.1:g.151847967C>A GRCh37
NC_000006.10:g.151889660C>A NCBI36
NG_021198.1:g.37793C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9486C>A MANE Select ENSP00000239374.6:n.58-9486C>A
ENST00000239374.7:c.58-9486C>A ENSP00000239374.6:n.58-9486C>A
NM_025059.3:c.58-9486C>A NP_079335.2:n.58-9486C>A
NM_025059.4:c.58-9486C>A MANE Select NP_079335.2:n.58-9486C>A
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