Canonical Allele Identifier: CA451867434

Gene: CCDC162P

Linked Data

• gnomAD v4: 6-109305595-A-T
• MyVariant Identifiers: chr6:g.109626798A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305595A>T , CM000668.2:g.109305595A>T	GRCh38
NC_000006.11:g.109626798A>T , CM000668.1:g.109626798A>T	GRCh37
NC_000006.10:g.109733491A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429614.6:n.323-364A>T
ENST00000689724.1:n.55-364A>T
ENST00000691019.1:n.505-364A>T
ENST00000691264.1:n.61-364A>T
ENST00000693346.1:n.55-364A>T
ENST00000368966.10:n.4200-364A>T
ENST00000638844.1:n.456-364A>T
ENST00000368966.8:n.456-364A>T
ENST00000422819.5:n.462-364A>T
ENST00000429614.5:n.323-364A>T
ENST00000615766.4:n.825-364A>T
NR_028595.1:n.323-364A>T
NR_152435.1:n.4168-364A>T