Canonical Allele Identifier: CA820830839
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1280443837
gnomAD v3: 6-151618236-T-C
gnomAD v4: 6-151618236-T-C
MyVariant Identifiers: chr6:g.151939371T>C (hg19) chr6:g.151618236T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618236T>C , CM000668.2:g.151618236T>C GRCh38
NC_000006.11:g.151939371T>C , CM000668.1:g.151939371T>C GRCh37
NC_000006.10:g.151981064T>C NCBI36
NG_021198.1:g.129197T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*89T>C MANE Select ENSP00000239374.6:n.*89T>C
ENST00000239374.7:c.*89T>C ENSP00000239374.6:n.*89T>C
NM_025059.3:c.*89T>C NP_079335.2:n.*89T>C
XM_011536147.1:c.*89T>C XP_011534449.1:n.*89T>C
XM_011536148.1:c.*89T>C XP_011534450.1:n.*89T>C
XM_011536147.2:c.*89T>C XP_011534449.1:n.*89T>C
XM_011536148.2:c.*89T>C XP_011534450.1:n.*89T>C
NM_025059.4:c.*89T>C MANE Select NP_079335.2:n.*89T>C
Search 100 bp 5'
Search 100 bp 3'