Canonical Allele Identifier: CA3712422
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs775267606
gnomAD v2: 6-31431706-T-A
gnomAD v3: 6-31463929-T-A
gnomAD v4: 6-31463929-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463929T>A , CM000668.2:g.31463929T>A GRCh38
NC_000006.11:g.31431706T>A , CM000668.1:g.31431706T>A GRCh37
NC_000006.10:g.31539685T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.659T>A