Canonical Allele Identifier: CA366067479
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936706T>A (hg19) chr6:g.151615571T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615571T>A , CM000668.2:g.151615571T>A GRCh38
NC_000006.11:g.151936706T>A , CM000668.1:g.151936706T>A GRCh37
NC_000006.10:g.151978399T>A NCBI36
NG_021198.1:g.126532T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1839T>A MANE Select ENSP00000239374.6:p.His613Gln
ENST00000239374.7:c.1839T>A ENSP00000239374.6:p.His613Gln
NM_025059.3:c.1839T>A NP_079335.2:p.His613Gln
XM_011536147.1:c.1857T>A XP_011534449.1:p.His619Gln
XM_011536148.1:c.1656T>A XP_011534450.1:p.His552Gln
XM_011536147.2:c.1857T>A XP_011534449.1:p.His619Gln
XM_011536148.2:c.1656T>A XP_011534450.1:p.His552Gln
XR_001743865.1:n.129+1150A>T
NM_025059.4:c.1839T>A MANE Select NP_079335.2:p.His613Gln
Search 100 bp 5'
Search 100 bp 3'