Canonical Allele Identifier: CA820813832
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1399597265
MyVariant Identifiers: chr6:g.151847946T>C (hg19) chr6:g.151526811T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526811T>C , CM000668.2:g.151526811T>C GRCh38
NC_000006.11:g.151847946T>C , CM000668.1:g.151847946T>C GRCh37
NC_000006.10:g.151889639T>C NCBI36
NG_021198.1:g.37772T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9507T>C MANE Select ENSP00000239374.6:n.58-9507T>C
ENST00000239374.7:c.58-9507T>C ENSP00000239374.6:n.58-9507T>C
NM_025059.3:c.58-9507T>C NP_079335.2:n.58-9507T>C
NM_025059.4:c.58-9507T>C MANE Select NP_079335.2:n.58-9507T>C
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