Canonical Allele Identifier: CA136868783

Gene: HCP5

Linked Data

• dbSNP Id: rs766640467
• gnomAD v2: 6-31432056-CCG-C
• gnomAD v3: 6-31464279-CCG-C
• gnomAD v4: 6-31464279-CCG-C
• MyVariant Identifiers: chr6:g.31432057_31432058del (hg19) ; chr6:g.31464280_31464281del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464281_31464282del , CM000668.2:g.31464281_31464282del	GRCh38
NC_000006.11:g.31432058_31432059del , CM000668.1:g.31432058_31432059del	GRCh37
NC_000006.10:g.31540037_31540038del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1011_1012del