Canonical Allele Identifier: CA2580593401
Gene: CCDC162P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109277761G= , CM000668.2:g.109277761G= GRCh38
NC_000006.11:g.109598964G= , CM000668.1:g.109598964G= GRCh37
NC_000006.10:g.109705657G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368966.10:n.3277-4806G=
XM_011535379.1:c.1909-4806G= XP_011533681.1:n.1909-4806G=
NR_152435.1:n.3360-4806G=