Canonical Allele Identifier: CA136868530

Gene: HCP5

Linked Data

• dbSNP Id: rs918002928
• gnomAD v2: 6-31431571-G-A
• gnomAD v4: 6-31463794-G-A
• MyVariant Identifiers: chr6:g.31431571G>A (hg19) ; chr6:g.31463794G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463794G>A , CM000668.2:g.31463794G>A	GRCh38
NC_000006.11:g.31431571G>A , CM000668.1:g.31431571G>A	GRCh37
NC_000006.10:g.31539550G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.524G>A