ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA712620491
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856397T>C
GRCh37
chr15:g.39148598T>C
Linked Data - Sequence & Population
gnomAD v3:
15:38856397 T / C
gnomAD v4:
chr15-38856397-T-C
Linked Data - NCBI & NCI
dbSNP:
1403817736
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856397T>C , CM000677.2:g.38856397T>C
GRCh38
NC_000015.9:g.39148598T>C , CM000677.1:g.39148598T>C
GRCh37
NC_000015.8:g.36935890T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'