Canonical Allele Identifier: CA449651732

Gene: HCP5

Linked Data

• dbSNP Id: rs1196375580
• MyVariant Identifiers: chr6:g.31432090G>C (hg19) ; chr6:g.31464313G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464313G>C , CM000668.2:g.31464313G>C	GRCh38
NC_000006.11:g.31432090G>C , CM000668.1:g.31432090G>C	GRCh37
NC_000006.10:g.31540069G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1043G>C