Canonical Allele Identifier: CA150138000
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs184009632
gnomAD v2: 6-151847949-A-G
gnomAD v3: 6-151526814-A-G
gnomAD v4: 6-151526814-A-G
MyVariant Identifiers: chr6:g.151847949A>G (hg19) chr6:g.151526814A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526814A>G , CM000668.2:g.151526814A>G GRCh38
NC_000006.11:g.151847949A>G , CM000668.1:g.151847949A>G GRCh37
NC_000006.10:g.151889642A>G NCBI36
NG_021198.1:g.37775A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9504A>G MANE Select ENSP00000239374.6:n.58-9504A>G
ENST00000239374.7:c.58-9504A>G ENSP00000239374.6:n.58-9504A>G
NM_025059.3:c.58-9504A>G NP_079335.2:n.58-9504A>G
NM_025059.4:c.58-9504A>G MANE Select NP_079335.2:n.58-9504A>G
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