Canonical Allele Identifier: CA451867433
Gene: CCDC162P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.109626797T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305594T>G , CM000668.2:g.109305594T>G GRCh38
NC_000006.11:g.109626797T>G , CM000668.1:g.109626797T>G GRCh37
NC_000006.10:g.109733490T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429614.6:n.323-365T>G
ENST00000689724.1:n.55-365T>G
ENST00000691019.1:n.505-365T>G
ENST00000691264.1:n.61-365T>G
ENST00000693346.1:n.55-365T>G
ENST00000368966.10:n.4200-365T>G
ENST00000638844.1:n.456-365T>G
ENST00000368966.8:n.456-365T>G
ENST00000422819.5:n.462-365T>G
ENST00000429614.5:n.323-365T>G
ENST00000615766.4:n.825-365T>G
NR_028595.1:n.323-365T>G
NR_152435.1:n.4168-365T>G