ClinGen Allele Registry
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Canonical Allele Identifier:
CA12994278
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.97858130T>C
GRCh37
chr9:g.100620412T>C
Linked Data - Sequence & Population
gnomAD v2:
9:100620412 T / C
gnomAD v3:
9:97858130 T / C
gnomAD v4:
chr9-97858130-T-C
Joint Max Group AF
0.86374093 (EAS)
Genomes Max Group AF
0.86374093 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4460498
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.97858130T>C , CM000671.2:g.97858130T>C
GRCh38
NC_000009.11:g.100620412T>C , CM000671.1:g.100620412T>C
GRCh37
NC_000009.10:g.99660233T>C
NCBI36
NG_011979.1:g.9876T>C
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