Canonical Allele Identifier: CA2679936505
Gene: CCDC162P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305607A>C , CM000668.2:g.109305607A>C GRCh38
NC_000006.11:g.109626810A>C , CM000668.1:g.109626810A>C GRCh37
NC_000006.10:g.109733503A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-352A>C
ENST00000689724.1:n.55-352A>C
ENST00000691019.1:n.505-352A>C
ENST00000691264.1:n.61-352A>C
ENST00000693346.1:n.55-352A>C
ENST00000368966.10:n.4200-352A>C
ENST00000638844.1:n.456-352A>C
ENST00000368966.8:n.456-352A>C
ENST00000422819.5:n.462-352A>C
ENST00000429614.5:n.323-352A>C
ENST00000615766.4:n.825-352A>C
NR_028595.1:n.323-352A>C
NR_152435.1:n.4168-352A>C