Canonical Allele Identifier: CA817055387
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1227067390
gnomAD v3: 6-109305761-C-T
gnomAD v4: 6-109305761-C-T
MyVariant Identifiers: chr6:g.109626964C>T (hg19) chr6:g.109305761C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305761C>T , CM000668.2:g.109305761C>T GRCh38
NC_000006.11:g.109626964C>T , CM000668.1:g.109626964C>T GRCh37
NC_000006.10:g.109733657C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-198C>T
ENST00000689724.1:n.55-198C>T
ENST00000691019.1:n.505-198C>T
ENST00000691264.1:n.61-198C>T
ENST00000693346.1:n.55-198C>T
ENST00000368966.10:n.4200-198C>T
ENST00000638844.1:n.456-198C>T
ENST00000368966.8:n.456-198C>T
ENST00000422819.5:n.462-198C>T
ENST00000429614.5:n.323-198C>T
ENST00000615766.4:n.825-198C>T
NR_028595.1:n.323-198C>T
NR_152435.1:n.4168-198C>T
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