Canonical Allele Identifier: CA566689594

Gene: HCP5

Linked Data

• dbSNP Id: rs1232634291
• gnomAD v2: 6-31431739-TC-T
• gnomAD v3: 6-31463962-TC-T
• gnomAD v4: 6-31463962-TC-T
• MyVariant Identifiers: chr6:g.31431740del (hg19) ; chr6:g.31463963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463963del , CM000668.2:g.31463963del	GRCh38
NC_000006.11:g.31431740del , CM000668.1:g.31431740del	GRCh37
NC_000006.10:g.31539719del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.693del