Canonical Allele Identifier: CA449652294

Gene: HCP5

Linked Data

• dbSNP Id: rs1762880262
• MyVariant Identifiers: chr6:g.31432190A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464413A>C , CM000668.2:g.31464413A>C	GRCh38
NC_000006.11:g.31432190A>C , CM000668.1:g.31432190A>C	GRCh37
NC_000006.10:g.31540169A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1143A>C