Canonical Allele Identifier: CA108748938
Gene:
MyVariant.info:
GRCh38 chr4:g.154562556G>A
GRCh37 chr4:g.155483708G>A
gnomAD v2:
4:155483708 G / A
gnomAD v3:
4:154562556 G / A
gnomAD v4:
chr4-154562556-G-A
Joint Max Group AF 0.2066928 (EAS)
Genomes Max Group AF 0.2066928 (EAS)
ClinVar RCV:
RCV000017814
ClinVar Variation:
16388
dbSNP:
1800790
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154562556G>A , CM000666.2:g.154562556G>A GRCh38
NC_000004.11:g.155483708G>A , CM000666.1:g.155483708G>A GRCh37
NC_000004.10:g.155703158G>A NCBI36
NG_008833.1:g.4577G>A , LRG_558:g.4577G>A
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