Canonical Allele Identifier: CA451867412

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1776647992
• gnomAD v4: 6-109305587-T-C
• MyVariant Identifiers: chr6:g.109626790T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305587T>C , CM000668.2:g.109305587T>C	GRCh38
NC_000006.11:g.109626790T>C , CM000668.1:g.109626790T>C	GRCh37
NC_000006.10:g.109733483T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429614.6:n.323-372T>C
ENST00000689724.1:n.55-372T>C
ENST00000691019.1:n.505-372T>C
ENST00000691264.1:n.61-372T>C
ENST00000693346.1:n.55-372T>C
ENST00000368966.10:n.4200-372T>C
ENST00000638844.1:n.456-372T>C
ENST00000368966.8:n.456-372T>C
ENST00000422819.5:n.462-372T>C
ENST00000429614.5:n.323-372T>C
ENST00000615766.4:n.825-372T>C
NR_028595.1:n.323-372T>C
NR_152435.1:n.4168-372T>C