Canonical Allele Identifier: CA449650450

Gene: HCP5

Linked Data

• dbSNP Id: rs768103863
• MyVariant Identifiers: chr6:g.31431822C>G (hg19) ; chr6:g.31464045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464045C>G , CM000668.2:g.31464045C>G	GRCh38
NC_000006.11:g.31431822C>G , CM000668.1:g.31431822C>G	GRCh37
NC_000006.10:g.31539801C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.775C>G