ClinGen Allele Registry
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Canonical Allele Identifier:
CA686004747
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.17220805G>T
GRCh37
chr12:g.17373739G>T
Linked Data - Sequence & Population
gnomAD v3:
12:17220805 G / T
gnomAD v4:
chr12-17220805-G-T
Linked Data - NCBI & NCI
dbSNP:
9971637
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.17220805G>T , CM000674.2:g.17220805G>T
GRCh38
NC_000012.11:g.17373739G>T , CM000674.1:g.17373739G>T
GRCh37
NC_000012.10:g.17265006G>T
NCBI36
Search 100 bp 5'
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