ClinGen Allele Registry
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Canonical Allele Identifier:
CA600564198
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.81524050T>A
GRCh37
chr11:g.81235092T>A
Linked Data - Sequence & Population
gnomAD v2:
11:81235092 T / A
gnomAD v3:
11:81524050 T / A
gnomAD v4:
chr11-81524050-T-A
Linked Data - NCBI & NCI
dbSNP:
1355640273
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.81524050T>A , CM000673.2:g.81524050T>A
GRCh38
NC_000011.9:g.81235092T>A , CM000673.1:g.81235092T>A
GRCh37
NC_000011.8:g.80912740T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'