Canonical Allele Identifier: CA449649361
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463725-G-T
MyVariant Identifiers: chr6:g.31431502G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463725G>T , CM000668.2:g.31463725G>T GRCh38
NC_000006.11:g.31431502G>T , CM000668.1:g.31431502G>T GRCh37
NC_000006.10:g.31539481G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.455G>T
Search 100 bp 5'
Search 100 bp 3'