Canonical Allele Identifier: CA452969745
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs371023882
gnomAD v2: 6-151936727-A-G
gnomAD v3: 6-151615592-A-G
gnomAD v4: 6-151615592-A-G
MyVariant Identifiers: chr6:g.151936727A>G (hg19) chr6:g.151615592A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615592A>G , CM000668.2:g.151615592A>G GRCh38
NC_000006.11:g.151936727A>G , CM000668.1:g.151936727A>G GRCh37
NC_000006.10:g.151978420A>G NCBI36
NG_021198.1:g.126553A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1860A>G MANE Select ENSP00000239374.6:p.Glu620=
ENST00000239374.7:c.1860A>G ENSP00000239374.6:p.Glu620=
NM_025059.3:c.1860A>G NP_079335.2:p.Glu620=
XM_011536147.1:c.1878A>G XP_011534449.1:p.Glu626=
XM_011536148.1:c.1677A>G XP_011534450.1:p.Glu559=
XM_011536147.2:c.1878A>G XP_011534449.1:p.Glu626=
XM_011536148.2:c.1677A>G XP_011534450.1:p.Glu559=
XR_001743865.1:n.129+1129T>C
NM_025059.4:c.1860A>G MANE Select NP_079335.2:p.Glu620=
Search 100 bp 5'
Search 100 bp 3'