ClinGen Allele Registry
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Canonical Allele Identifier:
CA728695972
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186681553T>G
GRCh37
chr1:g.186650685T>G
Linked Data - Sequence & Population
gnomAD v3:
1:186681553 T / G
gnomAD v4:
chr1-186681553-T-G
Linked Data - NCBI & NCI
dbSNP:
1191742996
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186681553T>G , CM000663.2:g.186681553T>G
GRCh38
NC_000001.10:g.186650685T>G , CM000663.1:g.186650685T>G
GRCh37
NC_000001.9:g.184917308T>G
NCBI36
NG_028206.2:g.3875A>C
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