Canonical Allele Identifier: CA449650064

Gene: HCP5

Linked Data

• dbSNP Id: rs2113963479
• MyVariant Identifiers: chr6:g.31431688C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463911C>G , CM000668.2:g.31463911C>G	GRCh38
NC_000006.11:g.31431688C>G , CM000668.1:g.31431688C>G	GRCh37
NC_000006.10:g.31539667C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.641C>G