Canonical Allele Identifier: CA817055418
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1466313922
gnomAD v3: 6-109305824-G-T
gnomAD v4: 6-109305824-G-T
MyVariant Identifiers: chr6:g.109627027G>T (hg19) chr6:g.109305824G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305824G>T , CM000668.2:g.109305824G>T GRCh38
NC_000006.11:g.109627027G>T , CM000668.1:g.109627027G>T GRCh37
NC_000006.10:g.109733720G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-135G>T
ENST00000689724.1:n.55-135G>T
ENST00000691019.1:n.505-135G>T
ENST00000691264.1:n.61-135G>T
ENST00000693346.1:n.55-135G>T
ENST00000368966.10:n.4200-135G>T
ENST00000638844.1:n.456-135G>T
ENST00000368966.8:n.456-135G>T
ENST00000422819.5:n.462-135G>T
ENST00000429614.5:n.323-135G>T
ENST00000615766.4:n.825-135G>T
NR_028595.1:n.323-135G>T
NR_152435.1:n.4168-135G>T
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