Canonical Allele Identifier: CA136868821
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs200006493
MyVariant Identifiers: chr6:g.31432168del (hg19) chr6:g.31464391del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464391del , CM000668.2:g.31464391del GRCh38
NC_000006.11:g.31432168del , CM000668.1:g.31432168del GRCh37
NC_000006.10:g.31540147del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1121del
Search 100 bp 5'
Search 100 bp 3'