ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA182463538
Gene:
Linked Data
dbSNP Id:
rs376619159
MyVariant Identifiers:
chr8:g.98281807A>C (hg19)
chr8:g.97269579A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.97269579A>C , CM000670.2:g.97269579A>C
GRCh38
NC_000008.10:g.98281807A>C , CM000670.1:g.98281807A>C
GRCh37
NC_000008.9:g.98350983A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125390.1:n.471+149491T>G
Search 100 bp 5'
Search 100 bp 3'