Canonical Allele Identifier: CA3712424
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs2255223
ExAC: 6:31431723 G / A
gnomAD v2: 6-31431723-G-A
gnomAD v3: 6-31463946-G-A
gnomAD v4: 6-31463946-G-A
MyVariant Identifiers: chr6:g.31431723G>A (hg19) chr6:g.31463946G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463946G>A , CM000668.2:g.31463946G>A GRCh38
NC_000006.11:g.31431723G>A , CM000668.1:g.31431723G>A GRCh37
NC_000006.10:g.31539702G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.676G>A
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