Canonical Allele Identifier: CA566689595

Gene: HCP5

Linked Data

• dbSNP Id: rs1223998935
• gnomAD v2: 6-31431869-AGT-A
• gnomAD v4: 6-31464092-AGT-A
• MyVariant Identifiers: chr6:g.31431870_31431871del (hg19) ; chr6:g.31464093_31464094del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464096_31464097del , CM000668.2:g.31464096_31464097del	GRCh38
NC_000006.11:g.31431873_31431874del , CM000668.1:g.31431873_31431874del	GRCh37
NC_000006.10:g.31539852_31539853del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.826_827del