Canonical Allele Identifier: CA449650847

Gene: HCP5

Linked Data

• dbSNP Id: rs1278974087
• COSMIC: COSN22087036
• MyVariant Identifiers: chr6:g.31431910G>A (hg19) ; chr6:g.31464133G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464133G>A , CM000668.2:g.31464133G>A	GRCh38
NC_000006.11:g.31431910G>A , CM000668.1:g.31431910G>A	GRCh37
NC_000006.10:g.31539889G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.863G>A