Canonical Allele Identifier: CA1672929526
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526652A= , CM000668.2:g.151526652A= GRCh38
NC_000006.11:g.151847787A= , CM000668.1:g.151847787A= GRCh37
NC_000006.10:g.151889480A= NCBI36
NG_021198.1:g.37613A=

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9666A= MANE Select ENSP00000239374.6:n.58-9666A=
ENST00000239374.7:c.58-9666A= ENSP00000239374.6:n.58-9666A=
NM_025059.3:c.58-9666A= NP_079335.2:n.58-9666A=
NM_025059.4:c.58-9666A= MANE Select NP_079335.2:n.58-9666A=
Search 100 bp 5'
Search 100 bp 3'