Canonical Allele Identifier: CA136868835
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs17206897
gnomAD v2: 6-31432209-G-A
gnomAD v3: 6-31464432-G-A
gnomAD v4: 6-31464432-G-A
MyVariant Identifiers: chr6:g.31432209G>A (hg19) chr6:g.31464432G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464432G>A , CM000668.2:g.31464432G>A GRCh38
NC_000006.11:g.31432209G>A , CM000668.1:g.31432209G>A GRCh37
NC_000006.10:g.31540188G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1162G>A
Search 100 bp 5'
Search 100 bp 3'