Canonical Allele Identifier: CA3712435
Gene: HCP5 HGNC NCBI

Linked Data

ClinVar Variation Id: 14910
dbSNP Id: rs2395029
gnomAD v2: 6-31431780-T-G
gnomAD v3: 6-31464003-T-G
gnomAD v4: 6-31464003-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464003T>G , CM000668.2:g.31464003T>G GRCh38
NC_000006.11:g.31431780T>G , CM000668.1:g.31431780T>G GRCh37
NC_000006.10:g.31539759T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.733T>G