Canonical Allele Identifier: CA2679936588
Gene: CCDC162P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305718G>T , CM000668.2:g.109305718G>T GRCh38
NC_000006.11:g.109626921G>T , CM000668.1:g.109626921G>T GRCh37
NC_000006.10:g.109733614G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-241G>T
ENST00000689724.1:n.55-241G>T
ENST00000691019.1:n.505-241G>T
ENST00000691264.1:n.61-241G>T
ENST00000693346.1:n.55-241G>T
ENST00000368966.10:n.4200-241G>T
ENST00000638844.1:n.456-241G>T
ENST00000368966.8:n.456-241G>T
ENST00000422819.5:n.462-241G>T
ENST00000429614.5:n.323-241G>T
ENST00000615766.4:n.825-241G>T
NR_028595.1:n.323-241G>T
NR_152435.1:n.4168-241G>T