Canonical Allele Identifier: CA150156384
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs778282784
gnomAD v4: 6-151618721-A-C
MyVariant Identifiers: chr6:g.151939856A>C (hg19) chr6:g.151618721A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618721A>C , CM000668.2:g.151618721A>C GRCh38
NC_000006.11:g.151939856A>C , CM000668.1:g.151939856A>C GRCh37
NC_000006.10:g.151981549A>C NCBI36
NG_021198.1:g.129682A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*574A>C MANE Select ENSP00000239374.6:n.*574A>C
ENST00000239374.7:c.*574A>C ENSP00000239374.6:n.*574A>C
NM_025059.3:c.*574A>C NP_079335.2:n.*574A>C
XM_011536147.1:c.*574A>C XP_011534449.1:n.*574A>C
XM_011536148.1:c.*574A>C XP_011534450.1:n.*574A>C
XM_011536147.2:c.*574A>C XP_011534449.1:n.*574A>C
XM_011536148.2:c.*574A>C XP_011534450.1:n.*574A>C
NM_025059.4:c.*574A>C MANE Select NP_079335.2:n.*574A>C
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