Canonical Allele Identifier: CA566689593

Gene: HCP5

Linked Data

• dbSNP Id: rs1242143890
• gnomAD v2: 6-31431729-ACTC-A
• gnomAD v3: 6-31463952-ACTC-A
• gnomAD v4: 6-31463952-ACTC-A
• MyVariant Identifiers: chr6:g.31431730_31431732del (hg19) ; chr6:g.31463953_31463955del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463956_31463958del , CM000668.2:g.31463956_31463958del	GRCh38
NC_000006.11:g.31431733_31431735del , CM000668.1:g.31431733_31431735del	GRCh37
NC_000006.10:g.31539712_31539714del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.686_688del