Canonical Allele Identifier: CA150160183
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs944519233
MyVariant Identifiers: chr6:g.151901438A>G (hg19) chr6:g.151580303A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580303A>G , CM000668.2:g.151580303A>G GRCh38
NC_000006.11:g.151901438A>G , CM000668.1:g.151901438A>G GRCh37
NC_000006.10:g.151943131A>G NCBI36
NG_021198.1:g.91264A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5586A>G MANE Select ENSP00000239374.6:n.1093-5586A>G
ENST00000239374.7:c.1093-5586A>G ENSP00000239374.6:n.1093-5586A>G
NM_025059.3:c.1093-5586A>G NP_079335.2:n.1093-5586A>G
XM_011536147.1:c.1111-5586A>G XP_011534449.1:n.1111-5586A>G
XM_011536148.1:c.1110+6812A>G XP_011534450.1:n.1110+6812A>G
XM_011536147.2:c.1111-5586A>G XP_011534449.1:n.1111-5586A>G
XM_011536148.2:c.1110+6812A>G XP_011534450.1:n.1110+6812A>G
NM_025059.4:c.1093-5586A>G MANE Select NP_079335.2:n.1093-5586A>G
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