Canonical Allele Identifier: CA820809513
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1348250848
MyVariant Identifiers: chr6:g.151901351T>A (hg19) chr6:g.151580216T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580216T>A , CM000668.2:g.151580216T>A GRCh38
NC_000006.11:g.151901351T>A , CM000668.1:g.151901351T>A GRCh37
NC_000006.10:g.151943044T>A NCBI36
NG_021198.1:g.91177T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5673T>A MANE Select ENSP00000239374.6:n.1093-5673T>A
ENST00000239374.7:c.1093-5673T>A ENSP00000239374.6:n.1093-5673T>A
NM_025059.3:c.1093-5673T>A NP_079335.2:n.1093-5673T>A
XM_011536147.1:c.1111-5673T>A XP_011534449.1:n.1111-5673T>A
XM_011536148.1:c.1110+6725T>A XP_011534450.1:n.1110+6725T>A
XM_011536147.2:c.1111-5673T>A XP_011534449.1:n.1111-5673T>A
XM_011536148.2:c.1110+6725T>A XP_011534450.1:n.1110+6725T>A
NM_025059.4:c.1093-5673T>A MANE Select NP_079335.2:n.1093-5673T>A
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