Canonical Allele Identifier: CA2712487408

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1776645514

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305294G>A , CM000668.2:g.109305294G>A	GRCh38
NC_000006.11:g.109626497G>A , CM000668.1:g.109626497G>A	GRCh37
NC_000006.10:g.109733190G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-665G>A
ENST00000689724.1:n.55-665G>A
ENST00000691019.1:n.505-665G>A
ENST00000691264.1:n.61-665G>A
ENST00000693346.1:n.55-665G>A
ENST00000368966.10:n.4200-665G>A
ENST00000638844.1:n.456-665G>A
ENST00000368966.8:n.456-665G>A
ENST00000422819.5:n.462-665G>A
ENST00000429614.5:n.323-665G>A
ENST00000615766.4:n.825-665G>A
NR_028595.1:n.323-665G>A
NR_152435.1:n.4168-665G>A