Canonical Allele Identifier: CA136868794
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1013532609
gnomAD v3: 6-31464337-ATTC-A
gnomAD v4: 6-31464337-ATTC-A
MyVariant Identifiers: chr6:g.31432115_31432117del (hg19) chr6:g.31464338_31464340del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464340_31464342del , CM000668.2:g.31464340_31464342del GRCh38
NC_000006.11:g.31432117_31432119del , CM000668.1:g.31432117_31432119del GRCh37
NC_000006.10:g.31540096_31540098del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1070_1072del
Search 100 bp 5'
Search 100 bp 3'