Canonical Allele Identifier: CA817055204

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1417127797
• MyVariant Identifiers: chr6:g.109626551G>T (hg19) ; chr6:g.109305348G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305348G>T , CM000668.2:g.109305348G>T	GRCh38
NC_000006.11:g.109626551G>T , CM000668.1:g.109626551G>T	GRCh37
NC_000006.10:g.109733244G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-611G>T
ENST00000689724.1:n.55-611G>T
ENST00000691019.1:n.505-611G>T
ENST00000691264.1:n.61-611G>T
ENST00000693346.1:n.55-611G>T
ENST00000368966.10:n.4200-611G>T
ENST00000638844.1:n.456-611G>T
ENST00000368966.8:n.456-611G>T
ENST00000422819.5:n.462-611G>T
ENST00000429614.5:n.323-611G>T
ENST00000615766.4:n.825-611G>T
NR_028595.1:n.323-611G>T
NR_152435.1:n.4168-611G>T