ClinGen Allele Registry
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Canonical Allele Identifier:
CA449651602
Gene: HCP5
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr6:g.31432068T>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31464291T>A , CM000668.2:g.31464291T>A
GRCh38
NC_000006.11:g.31432068T>A , CM000668.1:g.31432068T>A
GRCh37
NC_000006.10:g.31540047T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040662.1:n.1021T>A
Search 100 bp 5'
Search 100 bp 3'