Canonical Allele Identifier: CA136868667
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs201060991
gnomAD v3: 6-31463963-C-A
gnomAD v4: 6-31463963-C-A
MyVariant Identifiers: chr6:g.31431740C>A (hg19) chr6:g.31463963C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463963C>A , CM000668.2:g.31463963C>A GRCh38
NC_000006.11:g.31431740C>A , CM000668.1:g.31431740C>A GRCh37
NC_000006.10:g.31539719C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.693C>A
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