Canonical Allele Identifier: CA14456291
Gene:
MyVariant.info:
GRCh38 chr17:g.47731462T>C
GRCh37 chr17:g.45808828T>C
gnomAD v2:
17:45808828 T / C
gnomAD v3:
17:47731462 T / C
gnomAD v4:
chr17-47731462-T-C
Joint Max Group AF 0.37280685 (SAS)
Genomes Max Group AF 0.37280685 (SAS)
ClinVar RCV:
RCV000005646
RCV000005647
ClinVar Variation:
5321
dbSNP:
4794067
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47731462T>C , CM000679.2:g.47731462T>C GRCh38
NC_000017.10:g.45808828T>C , CM000679.1:g.45808828T>C GRCh37
NC_000017.9:g.43163827T>C NCBI36
NG_012166.1:g.3219T>C
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