Canonical Allele Identifier: CA2712487676
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1776648152

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305599A>G , CM000668.2:g.109305599A>G GRCh38
NC_000006.11:g.109626802A>G , CM000668.1:g.109626802A>G GRCh37
NC_000006.10:g.109733495A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-360A>G
ENST00000689724.1:n.55-360A>G
ENST00000691019.1:n.505-360A>G
ENST00000691264.1:n.61-360A>G
ENST00000693346.1:n.55-360A>G
ENST00000368966.10:n.4200-360A>G
ENST00000638844.1:n.456-360A>G
ENST00000368966.8:n.456-360A>G
ENST00000422819.5:n.462-360A>G
ENST00000429614.5:n.323-360A>G
ENST00000615766.4:n.825-360A>G
NR_028595.1:n.323-360A>G
NR_152435.1:n.4168-360A>G