Canonical Allele Identifier: CA150138053
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs546900440
gnomAD v2: 6-151848061-C-T
gnomAD v3: 6-151526926-C-T
gnomAD v4: 6-151526926-C-T
MyVariant Identifiers: chr6:g.151848061C>T (hg19) chr6:g.151526926C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526926C>T , CM000668.2:g.151526926C>T GRCh38
NC_000006.11:g.151848061C>T , CM000668.1:g.151848061C>T GRCh37
NC_000006.10:g.151889754C>T NCBI36
NG_021198.1:g.37887C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9392C>T MANE Select ENSP00000239374.6:n.58-9392C>T
ENST00000239374.7:c.58-9392C>T ENSP00000239374.6:n.58-9392C>T
NM_025059.3:c.58-9392C>T NP_079335.2:n.58-9392C>T
NM_025059.4:c.58-9392C>T MANE Select NP_079335.2:n.58-9392C>T
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