ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA448749485
Gene: PERPP3
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh37
chr6:g.16161425A>C
Linked Data - NCBI & NCI
dbSNP:
6924995
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.16161194A>C , CM000668.2:g.16161194A>C
GRCh38
NC_000006.11:g.16161425A>C , CM000668.1:g.16161425A>C
GRCh37
NC_000006.10:g.16269404A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000407522.1:n.269A>C
Search 100 bp 5'
Search 100 bp 3'