ClinGen Allele Registry
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Canonical Allele Identifier:
CA496645466
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh37
chr16:g.74088091T>A
Linked Data - Sequence & Population
gnomAD v3:
16:74054192 T / A
gnomAD v4:
chr16-74054192-T-A
Linked Data - NCBI & NCI
dbSNP:
2387084
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.74054192T>A , CM000678.2:g.74054192T>A
GRCh38
NC_000016.9:g.74088091T>A , CM000678.1:g.74088091T>A
GRCh37
NC_000016.8:g.72645592T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'