Canonical Allele Identifier: CA1672965994
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs112675667
gnomAD v4: 6-151618216-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618216T>C , CM000668.2:g.151618216T>C GRCh38
NC_000006.11:g.151939351T>C , CM000668.1:g.151939351T>C GRCh37
NC_000006.10:g.151981044T>C NCBI36
NG_021198.1:g.129177T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*69T>C MANE Select ENSP00000239374.6:n.*69T>C
ENST00000239374.7:c.*69T>C ENSP00000239374.6:n.*69T>C
NM_025059.3:c.*69T>C NP_079335.2:n.*69T>C
XM_011536147.1:c.*69T>C XP_011534449.1:n.*69T>C
XM_011536148.1:c.*69T>C XP_011534450.1:n.*69T>C
XM_011536147.2:c.*69T>C XP_011534449.1:n.*69T>C
XM_011536148.2:c.*69T>C XP_011534450.1:n.*69T>C
NM_025059.4:c.*69T>C MANE Select NP_079335.2:n.*69T>C
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