Canonical Allele Identifier: CA2677964764
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463370-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463370G>T , CM000668.2:g.31463370G>T GRCh38
NC_000006.11:g.31431147G>T , CM000668.1:g.31431147G>T GRCh37
NC_000006.10:g.31539126G>T NCBI36

Transcript Alleles

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