Canonical Allele Identifier: CA4052000
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs758205934
ExAC: 6:151936824 A / G
gnomAD v2: 6-151936824-A-G
gnomAD v3: 6-151615689-A-G
gnomAD v4: 6-151615689-A-G
MyVariant Identifiers: chr6:g.151936824A>G (hg19) chr6:g.151615689A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615689A>G , CM000668.2:g.151615689A>G GRCh38
NC_000006.11:g.151936824A>G , CM000668.1:g.151936824A>G GRCh37
NC_000006.10:g.151978517A>G NCBI36
NG_021198.1:g.126650A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+10A>G MANE Select ENSP00000239374.6:n.1947+10A>G
ENST00000239374.7:c.1947+10A>G ENSP00000239374.6:n.1947+10A>G
NM_025059.3:c.1947+10A>G NP_079335.2:n.1947+10A>G
XM_011536147.1:c.1965+10A>G XP_011534449.1:n.1965+10A>G
XM_011536148.1:c.1764+10A>G XP_011534450.1:n.1764+10A>G
XM_011536147.2:c.1965+10A>G XP_011534449.1:n.1965+10A>G
XM_011536148.2:c.1764+10A>G XP_011534450.1:n.1764+10A>G
XR_001743865.1:n.129+1032T>C
NM_025059.4:c.1947+10A>G MANE Select NP_079335.2:n.1947+10A>G
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