ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA29987107
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.149920979A>T
GRCh37
chr1:g.149892872A>T
Linked Data - Sequence & Population
gnomAD v2:
1:149892872 A / T
gnomAD v3:
1:149920979 A / T
gnomAD v4:
chr1-149920979-A-T
Joint Max Group AF
0.00001973 (NFE)
Genomes Max Group AF
0.00001973 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11205277
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.149920979A>T , CM000663.2:g.149920979A>T
GRCh38
NC_000001.10:g.149892872A>T , CM000663.1:g.149892872A>T
GRCh37
NC_000001.9:g.148159496A>T
NCBI36
NG_050966.1:g.1904T>A
Search 100 bp 5'
Search 100 bp 3'