ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA205538142
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.30230903C>T
GRCh37
chr10:g.30519832C>T
Linked Data - Sequence & Population
gnomAD v2:
10:30519832 C / T
gnomAD v3:
10:30230903 C / T
gnomAD v4:
chr10-30230903-C-T
Joint Max Group AF
0.76977036 (NFE)
Genomes Max Group AF
0.76977036 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2995271
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.30230903C>T , CM000672.2:g.30230903C>T
GRCh38
NC_000010.10:g.30519832C>T , CM000672.1:g.30519832C>T
GRCh37
NC_000010.9:g.30559838C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120653.1:n.269-14C>T
Search 100 bp 5'
Search 100 bp 3'