Canonical Allele Identifier: CA2680801500
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs2115154580
gnomAD v4: 6-151618619-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618619A>G , CM000668.2:g.151618619A>G GRCh38
NC_000006.11:g.151939754A>G , CM000668.1:g.151939754A>G GRCh37
NC_000006.10:g.151981447A>G NCBI36
NG_021198.1:g.129580A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*472A>G MANE Select ENSP00000239374.6:n.*472A>G
ENST00000239374.7:c.*472A>G ENSP00000239374.6:n.*472A>G
NM_025059.3:c.*472A>G NP_079335.2:n.*472A>G
XM_011536147.1:c.*472A>G XP_011534449.1:n.*472A>G
XM_011536148.1:c.*472A>G XP_011534450.1:n.*472A>G
XM_011536147.2:c.*472A>G XP_011534449.1:n.*472A>G
XM_011536148.2:c.*472A>G XP_011534450.1:n.*472A>G
NM_025059.4:c.*472A>G MANE Select NP_079335.2:n.*472A>G
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