Canonical Allele Identifier: CA3712425
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs774796867
ExAC: 6:31431729 A / G
gnomAD v2: 6-31431729-A-G
gnomAD v4: 6-31463952-A-G
MyVariant Identifiers: chr6:g.31431729A>G (hg19) chr6:g.31431729_31431732delinsGCTC (hg19) chr6:g.31463952A>G (hg38) chr6:g.31463952_31463955delinsGCTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463952A>G , CM000668.2:g.31463952A>G GRCh38
NC_000006.11:g.31431729A>G , CM000668.1:g.31431729A>G GRCh37
NC_000006.10:g.31539708A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.682A>G
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