Canonical Allele Identifier: CA2679936654
Gene: CCDC162P HGNC NCBI

Linked Data

gnomAD v4: 6-109305850-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305850C>A , CM000668.2:g.109305850C>A GRCh38
NC_000006.11:g.109627053C>A , CM000668.1:g.109627053C>A GRCh37
NC_000006.10:g.109733746C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-109C>A
ENST00000689724.1:n.55-109C>A
ENST00000691019.1:n.505-109C>A
ENST00000691264.1:n.61-109C>A
ENST00000693346.1:n.55-109C>A
ENST00000368966.10:n.4200-109C>A
ENST00000638844.1:n.456-109C>A
ENST00000368966.8:n.456-109C>A
ENST00000422819.5:n.462-109C>A
ENST00000429614.5:n.323-109C>A
ENST00000615766.4:n.825-109C>A
NR_028595.1:n.323-109C>A
NR_152435.1:n.4168-109C>A
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