Canonical Allele Identifier: CA449650226

Gene: HCP5

Linked Data

• dbSNP Id: rs1214457888
• MyVariant Identifiers: chr6:g.31431746C>G (hg19) ; chr6:g.31463969C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463969C>G , CM000668.2:g.31463969C>G	GRCh38
NC_000006.11:g.31431746C>G , CM000668.1:g.31431746C>G	GRCh37
NC_000006.10:g.31539725C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.699C>G