Canonical Allele Identifier: CA1672962796
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1776956259
gnomAD v4: 6-151615747-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615747A>G , CM000668.2:g.151615747A>G GRCh38
NC_000006.11:g.151936882A>G , CM000668.1:g.151936882A>G GRCh37
NC_000006.10:g.151978575A>G NCBI36
NG_021198.1:g.126708A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+68A>G MANE Select ENSP00000239374.6:n.1947+68A>G
ENST00000239374.7:c.1947+68A>G ENSP00000239374.6:n.1947+68A>G
NM_025059.3:c.1947+68A>G NP_079335.2:n.1947+68A>G
XM_011536147.1:c.1965+68A>G XP_011534449.1:n.1965+68A>G
XM_011536148.1:c.1764+68A>G XP_011534450.1:n.1764+68A>G
XM_011536147.2:c.1965+68A>G XP_011534449.1:n.1965+68A>G
XM_011536148.2:c.1764+68A>G XP_011534450.1:n.1764+68A>G
XR_001743865.1:n.129+974T>C
NM_025059.4:c.1947+68A>G MANE Select NP_079335.2:n.1947+68A>G
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