Canonical Allele Identifier: CA1672929590
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1782417895
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526804C>T , CM000668.2:g.151526804C>T GRCh38
NC_000006.11:g.151847939C>T , CM000668.1:g.151847939C>T GRCh37
NC_000006.10:g.151889632C>T NCBI36
NG_021198.1:g.37765C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9514C>T MANE Select ENSP00000239374.6:n.58-9514C>T
ENST00000239374.7:c.58-9514C>T ENSP00000239374.6:n.58-9514C>T
NM_025059.3:c.58-9514C>T NP_079335.2:n.58-9514C>T
NM_025059.4:c.58-9514C>T MANE Select NP_079335.2:n.58-9514C>T
Search 100 bp 5'
Search 100 bp 3'