ClinGen Allele Registry
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Canonical Allele Identifier:
CA15896442
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.47731941T>C
GRCh37
chr17:g.45809307T>C
Linked Data - Sequence & Population
gnomAD v2:
17:45809307 T / C
gnomAD v3:
17:47731941 T / C
gnomAD v4:
chr17-47731941-T-C
Joint Max Group AF
0.19447248 (AMR)
Genomes Max Group AF
0.19447248 (AMR)
Linked Data - NCBI & NCI
dbSNP:
17250932
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.47731941T>C , CM000679.2:g.47731941T>C
GRCh38
NC_000017.10:g.45809307T>C , CM000679.1:g.45809307T>C
GRCh37
NC_000017.9:g.43164306T>C
NCBI36
NG_012166.1:g.3698T>C
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