Canonical Allele Identifier: CA136868818

Gene: HCP5

Linked Data

• dbSNP Id: rs76097004
• gnomAD v2: 6-31432164-TG-T
• gnomAD v3: 6-31464387-TG-T
• gnomAD v4: 6-31464387-TG-T
• MyVariant Identifiers: chr6:g.31432165del (hg19) ; chr6:g.31464388del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464390del , CM000668.2:g.31464390del	GRCh38
NC_000006.11:g.31432167del , CM000668.1:g.31432167del	GRCh37
NC_000006.10:g.31540146del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1120del