ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10576189
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39252525T>G
GRCh37
chr19:g.39743165T>G
Linked Data - Sequence & Population
gnomAD v2:
19:39743165 T / G
gnomAD v3:
19:39252525 T / G
gnomAD v4:
chr19-39252525-T-G
Joint Max Group AF
0.25149005 (AMR)
Genomes Max Group AF
0.25149005 (AMR)
Linked Data - NCBI & NCI
ClinVar Allele:
227802
ClinVar RCV:
RCV000211192
RCV000211316
RCV000835188
ClinVar Variation:
226027
dbSNP:
8099917
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39252525T>G , CM000681.2:g.39252525T>G
GRCh38
NC_000019.9:g.39743165T>G , CM000681.1:g.39743165T>G
GRCh37
NC_000019.8:g.44435005T>G
NCBI36
NG_055295.1:g.1332A>C
Search 100 bp 5'
Search 100 bp 3'