Canonical Allele Identifier: CA126965
Gene:
ClinVar RCV:
RCV000018417
RCV000018418
ClinVar Variation:
16916
dbSNP:
2740574
gnomAD v2:
7:99382096 C / T
gnomAD v3:
7:99784473 C / T
gnomAD v4:
chr7-99784473-C-T
Joint Max Group AF 0.9753573 (EAS)
Genomes Max Group AF 0.9753573 (EAS)
MyVariant.info:
GRCh38 chr7:g.99784473C>T
GRCh37 chr7:g.99382096C>T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99784473C>T , CM000669.2:g.99784473C>T GRCh38
NC_000007.13:g.99382096C>T , CM000669.1:g.99382096C>T GRCh37
NC_000007.12:g.99220032C>T NCBI36
NG_008421.1:g.4713G>A
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