Canonical Allele Identifier: CA150137999
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs974027341
gnomAD v3: 6-151526806-C-T
gnomAD v4: 6-151526806-C-T
MyVariant Identifiers: chr6:g.151847941C>T (hg19) chr6:g.151526806C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526806C>T , CM000668.2:g.151526806C>T GRCh38
NC_000006.11:g.151847941C>T , CM000668.1:g.151847941C>T GRCh37
NC_000006.10:g.151889634C>T NCBI36
NG_021198.1:g.37767C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9512C>T MANE Select ENSP00000239374.6:n.58-9512C>T
ENST00000239374.7:c.58-9512C>T ENSP00000239374.6:n.58-9512C>T
NM_025059.3:c.58-9512C>T NP_079335.2:n.58-9512C>T
NM_025059.4:c.58-9512C>T MANE Select NP_079335.2:n.58-9512C>T
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