ClinGen Allele Registry
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Canonical Allele Identifier:
CA449650344
Gene: HCP5
HGNC
NCBI
Linked Data
dbSNP Id:
rs1762861762
gnomAD v4:
6-31464011-G-A
MyVariant Identifiers:
chr6:g.31431788G>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31464011G>A , CM000668.2:g.31464011G>A
GRCh38
NC_000006.11:g.31431788G>A , CM000668.1:g.31431788G>A
GRCh37
NC_000006.10:g.31539767G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040662.1:n.741G>A
Search 100 bp 5'
Search 100 bp 3'