Canonical Allele Identifier: CA12356934
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1008083
gnomAD v2: 6-109626979-C-T
gnomAD v3: 6-109305776-C-T
gnomAD v4: 6-109305776-C-T
MyVariant Identifiers: chr6:g.109626979C>T (hg19) chr6:g.109305776C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305776C>T , CM000668.2:g.109305776C>T GRCh38
NC_000006.11:g.109626979C>T , CM000668.1:g.109626979C>T GRCh37
NC_000006.10:g.109733672C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-183C>T
ENST00000689724.1:n.55-183C>T
ENST00000691019.1:n.505-183C>T
ENST00000691264.1:n.61-183C>T
ENST00000693346.1:n.55-183C>T
ENST00000368966.10:n.4200-183C>T
ENST00000638844.1:n.456-183C>T
ENST00000368966.8:n.456-183C>T
ENST00000422819.5:n.462-183C>T
ENST00000429614.5:n.323-183C>T
ENST00000615766.4:n.825-183C>T
NR_028595.1:n.323-183C>T
NR_152435.1:n.4168-183C>T
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