Canonical Allele Identifier: CA12204086
Gene: CCDC162P HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1008084

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305762G>A , CM000668.2:g.109305762G>A GRCh38
NC_000006.11:g.109626965G>A , CM000668.1:g.109626965G>A GRCh37
NC_000006.10:g.109733658G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028595.1:n.323-197G>A
NR_152435.1:n.4168-197G>A
ENST00000368966.8:n.456-197G>A
ENST00000422819.5:n.462-197G>A
ENST00000429614.5:n.323-197G>A
ENST00000615766.4:n.825-197G>A