ClinGen Allele Registry
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Canonical Allele Identifier:
CA227368489
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102942545T>G
GRCh37
chr11:g.102813274T>G
Linked Data - NCBI & NCI
dbSNP:
1147071
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102942545T>G , CM000673.2:g.102942545T>G
GRCh38
NC_000011.9:g.102813274T>G , CM000673.1:g.102813274T>G
GRCh37
NC_000011.8:g.102318484T>G
NCBI36
NG_021404.1:g.18190A>C
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