Canonical Allele Identifier: CA150156230
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs55774154
gnomAD v2: 6-151939347-C-G
gnomAD v3: 6-151618212-C-G
gnomAD v4: 6-151618212-C-G
MyVariant Identifiers: chr6:g.151939347C>G (hg19) chr6:g.151618212C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618212C>G , CM000668.2:g.151618212C>G GRCh38
NC_000006.11:g.151939347C>G , CM000668.1:g.151939347C>G GRCh37
NC_000006.10:g.151981040C>G NCBI36
NG_021198.1:g.129173C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*65C>G MANE Select ENSP00000239374.6:n.*65C>G
ENST00000239374.7:c.*65C>G ENSP00000239374.6:n.*65C>G
NM_025059.3:c.*65C>G NP_079335.2:n.*65C>G
XM_011536147.1:c.*65C>G XP_011534449.1:n.*65C>G
XM_011536148.1:c.*65C>G XP_011534450.1:n.*65C>G
XM_011536147.2:c.*65C>G XP_011534449.1:n.*65C>G
XM_011536148.2:c.*65C>G XP_011534450.1:n.*65C>G
NM_025059.4:c.*65C>G MANE Select NP_079335.2:n.*65C>G
Search 100 bp 5'
Search 100 bp 3'