Canonical Allele Identifier: CA145763375
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs575236588
gnomAD v3: 6-109305816-G-A
gnomAD v4: 6-109305816-G-A
MyVariant Identifiers: chr6:g.109627019G>A (hg19) chr6:g.109305816G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305816G>A , CM000668.2:g.109305816G>A GRCh38
NC_000006.11:g.109627019G>A , CM000668.1:g.109627019G>A GRCh37
NC_000006.10:g.109733712G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-143G>A
ENST00000689724.1:n.55-143G>A
ENST00000691019.1:n.505-143G>A
ENST00000691264.1:n.61-143G>A
ENST00000693346.1:n.55-143G>A
ENST00000368966.10:n.4200-143G>A
ENST00000638844.1:n.456-143G>A
ENST00000368966.8:n.456-143G>A
ENST00000422819.5:n.462-143G>A
ENST00000429614.5:n.323-143G>A
ENST00000615766.4:n.825-143G>A
NR_028595.1:n.323-143G>A
NR_152435.1:n.4168-143G>A
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