ClinGen Allele Registry
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Canonical Allele Identifier:
CA449650094
Gene: HCP5
HGNC
NCBI
Linked Data
gnomAD v4:
6-31463921-G-T
MyVariant Identifiers:
chr6:g.31431698G>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31463921G>T , CM000668.2:g.31463921G>T
GRCh38
NC_000006.11:g.31431698G>T , CM000668.1:g.31431698G>T
GRCh37
NC_000006.10:g.31539677G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040662.1:n.651G>T
Search 100 bp 5'
Search 100 bp 3'