Canonical Allele Identifier: CA150156243
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs770956532
gnomAD v2: 6-151939354-C-A
gnomAD v3: 6-151618219-C-A
gnomAD v4: 6-151618219-C-A
MyVariant Identifiers: chr6:g.151939354C>A (hg19) chr6:g.151618219C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618219C>A , CM000668.2:g.151618219C>A GRCh38
NC_000006.11:g.151939354C>A , CM000668.1:g.151939354C>A GRCh37
NC_000006.10:g.151981047C>A NCBI36
NG_021198.1:g.129180C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*72C>A MANE Select ENSP00000239374.6:n.*72C>A
ENST00000239374.7:c.*72C>A ENSP00000239374.6:n.*72C>A
NM_025059.3:c.*72C>A NP_079335.2:n.*72C>A
XM_011536147.1:c.*72C>A XP_011534449.1:n.*72C>A
XM_011536148.1:c.*72C>A XP_011534450.1:n.*72C>A
XM_011536147.2:c.*72C>A XP_011534449.1:n.*72C>A
XM_011536148.2:c.*72C>A XP_011534450.1:n.*72C>A
NM_025059.4:c.*72C>A MANE Select NP_079335.2:n.*72C>A
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