Canonical Allele Identifier: CA136868831
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs894607392
gnomAD v4: 6-31464425-G-A
MyVariant Identifiers: chr6:g.31432202G>A (hg19) chr6:g.31464425G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464425G>A , CM000668.2:g.31464425G>A GRCh38
NC_000006.11:g.31432202G>A , CM000668.1:g.31432202G>A GRCh37
NC_000006.10:g.31540181G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1155G>A
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