Canonical Allele Identifier: CA3712427

Gene: HCP5

Linked Data

• dbSNP Id: rs762099595
• ExAC: 6:31431732 CCTCTT / C
• gnomAD v2: 6-31431732-CCTCTT-C
• gnomAD v3: 6-31463955-CCTCTT-C
• gnomAD v4: 6-31463955-CCTCTT-C
• MyVariant Identifiers: chr6:g.31431733_31431737del (hg19) ; chr6:g.31463956_31463960del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463959_31463963del , CM000668.2:g.31463959_31463963del	GRCh38
NC_000006.11:g.31431736_31431740del , CM000668.1:g.31431736_31431740del	GRCh37
NC_000006.10:g.31539715_31539719del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.689_693del