ClinGen Allele Registry
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Canonical Allele Identifier:
CA566352360
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31575287A>C
GRCh37
chr6:g.31543064A>C
Linked Data - Sequence & Population
gnomAD v2:
6:31543064 A / C
gnomAD v4:
chr6-31575287-A-C
Linked Data - NCBI & NCI
dbSNP:
56036015
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31575287A>C , CM000668.2:g.31575287A>C
GRCh38
NC_000006.11:g.31543064A>C , CM000668.1:g.31543064A>C
GRCh37
NC_000006.10:g.31651043A>C
NCBI36
NG_007462.1:g.4715A>C
NG_012010.1:g.8189A>C
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