Canonical Allele Identifier: CA571119440
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1412413501
gnomAD v2: 6-151847780-A-G
gnomAD v3: 6-151526645-A-G
gnomAD v4: 6-151526645-A-G
MyVariant Identifiers: chr6:g.151847780A>G (hg19) chr6:g.151526645A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526645A>G , CM000668.2:g.151526645A>G GRCh38
NC_000006.11:g.151847780A>G , CM000668.1:g.151847780A>G GRCh37
NC_000006.10:g.151889473A>G NCBI36
NG_021198.1:g.37606A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9673A>G MANE Select ENSP00000239374.6:n.58-9673A>G
ENST00000239374.7:c.58-9673A>G ENSP00000239374.6:n.58-9673A>G
NM_025059.3:c.58-9673A>G NP_079335.2:n.58-9673A>G
NM_025059.4:c.58-9673A>G MANE Select NP_079335.2:n.58-9673A>G
Search 100 bp 5'
Search 100 bp 3'