ClinGen Allele Registry
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Canonical Allele Identifier:
CA717929958
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.1081695A>C
GRCh37
chr16:g.1131695A>C
Linked Data - Sequence & Population
gnomAD v3:
16:1081695 A / C
gnomAD v4:
chr16-1081695-A-C
Linked Data - NCBI & NCI
dbSNP:
197056
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.1081695A>C , CM000678.2:g.1081695A>C
GRCh38
NC_000016.9:g.1131695A>C , CM000678.1:g.1131695A>C
GRCh37
NC_000016.8:g.1071696A>C
NCBI36
NG_016744.1:g.13940A>C
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