Canonical Allele Identifier: CA366069738
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151939258A>C (hg19) chr6:g.151618123A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618123A>C , CM000668.2:g.151618123A>C GRCh38
NC_000006.11:g.151939258A>C , CM000668.1:g.151939258A>C GRCh37
NC_000006.10:g.151980951A>C NCBI36
NG_021198.1:g.129084A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.2124A>C MANE Select ENSP00000239374.6:p.Gln708His
ENST00000239374.7:c.2124A>C ENSP00000239374.6:p.Gln708His
NM_025059.3:c.2124A>C NP_079335.2:p.Gln708His
XM_011536147.1:c.2142A>C XP_011534449.1:p.Gln714His
XM_011536148.1:c.1941A>C XP_011534450.1:p.Gln647His
XM_011536147.2:c.2142A>C XP_011534449.1:p.Gln714His
XM_011536148.2:c.1941A>C XP_011534450.1:p.Gln647His
NM_025059.4:c.2124A>C MANE Select NP_079335.2:p.Gln708His
Search 100 bp 5'
Search 100 bp 3'