Canonical Allele Identifier: CA571119438
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1371959295
gnomAD v2: 6-151847775-T-A
gnomAD v3: 6-151526640-T-A
gnomAD v4: 6-151526640-T-A
MyVariant Identifiers: chr6:g.151847775T>A (hg19) chr6:g.151526640T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526640T>A , CM000668.2:g.151526640T>A GRCh38
NC_000006.11:g.151847775T>A , CM000668.1:g.151847775T>A GRCh37
NC_000006.10:g.151889468T>A NCBI36
NG_021198.1:g.37601T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9678T>A MANE Select ENSP00000239374.6:n.58-9678T>A
ENST00000239374.7:c.58-9678T>A ENSP00000239374.6:n.58-9678T>A
NM_025059.3:c.58-9678T>A NP_079335.2:n.58-9678T>A
NM_025059.4:c.58-9678T>A MANE Select NP_079335.2:n.58-9678T>A
Search 100 bp 5'
Search 100 bp 3'