Canonical Allele Identifier: CA449650123

Gene: HCP5

Linked Data

• MyVariant Identifiers: chr6:g.31431709C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463932C>A , CM000668.2:g.31463932C>A	GRCh38
NC_000006.11:g.31431709C>A , CM000668.1:g.31431709C>A	GRCh37
NC_000006.10:g.31539688C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.662C>A