Canonical Allele Identifier: CA449651681
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762875195
gnomAD v3: 6-31464304-C-T
gnomAD v4: 6-31464304-C-T
MyVariant Identifiers: chr6:g.31432081C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464304C>T , CM000668.2:g.31464304C>T GRCh38
NC_000006.11:g.31432081C>T , CM000668.1:g.31432081C>T GRCh37
NC_000006.10:g.31540060C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1034C>T
Search 100 bp 5'
Search 100 bp 3'