Canonical Allele Identifier: CA150156246
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs776914311
gnomAD v4: 6-151618235-G-A
MyVariant Identifiers: chr6:g.151939370G>A (hg19) chr6:g.151618235G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618235G>A , CM000668.2:g.151618235G>A GRCh38
NC_000006.11:g.151939370G>A , CM000668.1:g.151939370G>A GRCh37
NC_000006.10:g.151981063G>A NCBI36
NG_021198.1:g.129196G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*88G>A MANE Select ENSP00000239374.6:n.*88G>A
ENST00000239374.7:c.*88G>A ENSP00000239374.6:n.*88G>A
NM_025059.3:c.*88G>A NP_079335.2:n.*88G>A
XM_011536147.1:c.*88G>A XP_011534449.1:n.*88G>A
XM_011536148.1:c.*88G>A XP_011534450.1:n.*88G>A
XM_011536147.2:c.*88G>A XP_011534449.1:n.*88G>A
XM_011536148.2:c.*88G>A XP_011534450.1:n.*88G>A
NM_025059.4:c.*88G>A MANE Select NP_079335.2:n.*88G>A
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