Canonical Allele Identifier: CA2712341673
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs9386791

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109287294C>G , CM000668.2:g.109287294C>G GRCh38
NC_000006.11:g.109608497C>G , CM000668.1:g.109608497C>G GRCh37
NC_000006.10:g.109715190C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368966.10:n.3773+776C>G
ENST00000615766.4:n.349+776C>G
NR_152435.1:n.3744+776C>G