Canonical Allele Identifier: CA15137531
Gene:
ClinVar RCV:
RCV000019529
ClinVar Variation:
17936
dbSNP:
5082
gnomAD v2:
1:161193683 G / A
gnomAD v3:
1:161223893 G / A
gnomAD v4:
chr1-161223893-G-A
Joint Max Group AF 0.8866638 (EAS)
Genomes Max Group AF 0.8866638 (EAS)
MyVariant.info:
GRCh38 chr1:g.161223893G>A
GRCh37 chr1:g.161193683G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161223893G>A , CM000663.2:g.161223893G>A GRCh38
NC_000001.10:g.161193683G>A , CM000663.1:g.161193683G>A GRCh37
NC_000001.9:g.159460307G>A NCBI36
NG_012043.1:g.4736C>T
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