ClinGen Allele Registry
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Canonical Allele Identifier:
CA891214142
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.172929296A>C
GRCh37
chr1:g.172898436A>C
Linked Data - Sequence & Population
gnomAD v3:
1:172929296 A / C
gnomAD v4:
chr1-172929296-A-C
Linked Data - NCBI & NCI
dbSNP:
1320256380
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.172929296A>C , CM000663.2:g.172929296A>C
GRCh38
NC_000001.10:g.172898436A>C , CM000663.1:g.172898436A>C
GRCh37
NC_000001.9:g.171165059A>C
NCBI36
Search 100 bp 5'
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