Canonical Allele Identifier: CA3712392
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs756177381
gnomAD v2: 6-31431507-T-G
gnomAD v3: 6-31463730-T-G
gnomAD v4: 6-31463730-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463730T>G , CM000668.2:g.31463730T>G GRCh38
NC_000006.11:g.31431507T>G , CM000668.1:g.31431507T>G GRCh37
NC_000006.10:g.31539486T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.460T>G