ClinGen Allele Registry
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Canonical Allele Identifier:
CA449650682
Gene: HCP5
HGNC
NCBI
Linked Data
gnomAD v4:
6-31464108-A-T
MyVariant Identifiers:
chr6:g.31431885A>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31464108A>T , CM000668.2:g.31464108A>T
GRCh38
NC_000006.11:g.31431885A>T , CM000668.1:g.31431885A>T
GRCh37
NC_000006.10:g.31539864A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040662.1:n.838A>T
Search 100 bp 5'
Search 100 bp 3'