Canonical Allele Identifier: CA571119445
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1214876184
gnomAD v2: 6-151847812-G-A
gnomAD v3: 6-151526677-G-A
gnomAD v4: 6-151526677-G-A
MyVariant Identifiers: chr6:g.151847812G>A (hg19) chr6:g.151526677G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526677G>A , CM000668.2:g.151526677G>A GRCh38
NC_000006.11:g.151847812G>A , CM000668.1:g.151847812G>A GRCh37
NC_000006.10:g.151889505G>A NCBI36
NG_021198.1:g.37638G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9641G>A MANE Select ENSP00000239374.6:n.58-9641G>A
ENST00000239374.7:c.58-9641G>A ENSP00000239374.6:n.58-9641G>A
NM_025059.3:c.58-9641G>A NP_079335.2:n.58-9641G>A
NM_025059.4:c.58-9641G>A MANE Select NP_079335.2:n.58-9641G>A
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