Canonical Allele Identifier: CA145763332

Gene: CCDC162P

Linked Data

• dbSNP Id: rs149296483
• gnomAD v2: 6-109626532-A-G
• gnomAD v3: 6-109305329-A-G
• gnomAD v4: 6-109305329-A-G
• MyVariant Identifiers: chr6:g.109626532A>G (hg19) ; chr6:g.109305329A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305329A>G , CM000668.2:g.109305329A>G	GRCh38
NC_000006.11:g.109626532A>G , CM000668.1:g.109626532A>G	GRCh37
NC_000006.10:g.109733225A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-630A>G
ENST00000689724.1:n.55-630A>G
ENST00000691019.1:n.505-630A>G
ENST00000691264.1:n.61-630A>G
ENST00000693346.1:n.55-630A>G
ENST00000368966.10:n.4200-630A>G
ENST00000638844.1:n.456-630A>G
ENST00000368966.8:n.456-630A>G
ENST00000422819.5:n.462-630A>G
ENST00000429614.5:n.323-630A>G
ENST00000615766.4:n.825-630A>G
NR_028595.1:n.323-630A>G
NR_152435.1:n.4168-630A>G