ClinGen Allele Registry
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Canonical Allele Identifier:
CA11792426
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.149980605G>A
GRCh37
chr4:g.150901757G>A
Linked Data - Sequence & Population
gnomAD v2:
4:150901757 G / A
gnomAD v3:
4:149980605 G / A
gnomAD v4:
chr4-149980605-G-A
Joint Max Group AF
0.2899079 (EAS)
Genomes Max Group AF
0.2899079 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11930273
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.149980605G>A , CM000666.2:g.149980605G>A
GRCh38
NC_000004.11:g.150901757G>A , CM000666.1:g.150901757G>A
GRCh37
NC_000004.10:g.151121207G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'