Canonical Allele Identifier: CA3712402

Gene: HCP5

Linked Data

• dbSNP Id: rs764730661
• ExAC: 6:31431562 GGGTGGCT / G
• gnomAD v2: 6-31431562-GGGTGGCT-G
• gnomAD v3: 6-31463785-GGGTGGCT-G
• gnomAD v4: 6-31463785-GGGTGGCT-G
• MyVariant Identifiers: chr6:g.31431563_31431569del (hg19) ; chr6:g.31463786_31463792del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463788_31463794del , CM000668.2:g.31463788_31463794del	GRCh38
NC_000006.11:g.31431565_31431571del , CM000668.1:g.31431565_31431571del	GRCh37
NC_000006.10:g.31539544_31539550del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.518_524del