Canonical Allele Identifier: CA449652383

Gene: HCP5

Linked Data

• dbSNP Id: rs1484395029
• gnomAD v3: 6-31464429-A-G
• gnomAD v4: 6-31464429-A-G
• MyVariant Identifiers: chr6:g.31432206A>G (hg19) ; chr6:g.31464429A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464429A>G , CM000668.2:g.31464429A>G	GRCh38
NC_000006.11:g.31432206A>G , CM000668.1:g.31432206A>G	GRCh37
NC_000006.10:g.31540185A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1159A>G