Canonical Allele Identifier: CA108749021
Gene:
MyVariant.info:
GRCh38 chr4:g.154562863C>T
GRCh37 chr4:g.155484015C>T
gnomAD v2:
4:155484015 C / T
gnomAD v3:
4:154562863 C / T
gnomAD v4:
chr4-154562863-C-T
Joint Max Group AF 0.22321864 (MID)
Genomes Max Group AF 0.20664111 (EAS)
Exomes Max Group AF 0.22170229 (MID)
ClinVar RCV:
RCV001619021
RCV001843309
ClinVar Variation:
1233839
dbSNP:
1800787
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154562863C>T , CM000666.2:g.154562863C>T GRCh38
NC_000004.11:g.155484015C>T , CM000666.1:g.155484015C>T GRCh37
NC_000004.10:g.155703465C>T NCBI36
NG_008833.1:g.4884C>T , LRG_558:g.4884C>T
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