Canonical Allele Identifier: CA449650167

Gene: HCP5

Linked Data

• dbSNP Id: rs1189194660
• MyVariant Identifiers: chr6:g.31431724A>C (hg19) ; chr6:g.31463947A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463947A>C , CM000668.2:g.31463947A>C	GRCh38
NC_000006.11:g.31431724A>C , CM000668.1:g.31431724A>C	GRCh37
NC_000006.10:g.31539703A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.677A>C