Canonical Allele Identifier: CA3712437
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs567550866
gnomAD v2: 6-31431792-T-C
gnomAD v3: 6-31464015-T-C
gnomAD v4: 6-31464015-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464015T>C , CM000668.2:g.31464015T>C GRCh38
NC_000006.11:g.31431792T>C , CM000668.1:g.31431792T>C GRCh37
NC_000006.10:g.31539771T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.745T>C