Canonical Allele Identifier: CA449652006

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464363-T-G
• MyVariant Identifiers: chr6:g.31432140T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464363T>G , CM000668.2:g.31464363T>G	GRCh38
NC_000006.11:g.31432140T>G , CM000668.1:g.31432140T>G	GRCh37
NC_000006.10:g.31540119T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1093T>G