Canonical Allele Identifier: CA449651612

Gene: HCP5

Linked Data

• dbSNP Id: rs1762874808
• MyVariant Identifiers: chr6:g.31432071T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464294T>A , CM000668.2:g.31464294T>A	GRCh38
NC_000006.11:g.31432071T>A , CM000668.1:g.31432071T>A	GRCh37
NC_000006.10:g.31540050T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1024T>A