ClinGen Allele Registry
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Canonical Allele Identifier:
CA721999201
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56960616C>G
GRCh37
chr16:g.56994528C>G
Linked Data - Sequence & Population
gnomAD v4:
chr16-56960616-C-G
Linked Data - NCBI & NCI
dbSNP:
17231506
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56960616C>G , CM000678.2:g.56960616C>G
GRCh38
NC_000016.9:g.56994528C>G , CM000678.1:g.56994528C>G
GRCh37
NC_000016.8:g.55552029C>G
NCBI36
NG_008952.1:g.3694C>G
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