Canonical Allele Identifier: CA2679936511

Gene: CCDC162P

Linked Data

• gnomAD v4: 6-109305624-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305624T>C , CM000668.2:g.109305624T>C	GRCh38
NC_000006.11:g.109626827T>C , CM000668.1:g.109626827T>C	GRCh37
NC_000006.10:g.109733520T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-335T>C
ENST00000689724.1:n.55-335T>C
ENST00000691019.1:n.505-335T>C
ENST00000691264.1:n.61-335T>C
ENST00000693346.1:n.55-335T>C
ENST00000368966.10:n.4200-335T>C
ENST00000638844.1:n.456-335T>C
ENST00000368966.8:n.456-335T>C
ENST00000422819.5:n.462-335T>C
ENST00000429614.5:n.323-335T>C
ENST00000615766.4:n.825-335T>C
NR_028595.1:n.323-335T>C
NR_152435.1:n.4168-335T>C