Canonical Allele Identifier: CA2677964758
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463362-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463362T>C , CM000668.2:g.31463362T>C GRCh38
NC_000006.11:g.31431139T>C , CM000668.1:g.31431139T>C GRCh37
NC_000006.10:g.31539118T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.101-9T>C