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Canonical Allele Identifier:
CA13484145
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.48212805C>T
GRCh37
chr11:g.48234357C>T
Linked Data - Sequence & Population
gnomAD v2:
11:48234357 C / T
gnomAD v3:
11:48212805 C / T
gnomAD v4:
chr11-48212805-C-T
Joint Max Group AF
0.21706149 (SAS)
Genomes Max Group AF
0.21706149 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11039588
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.48212805C>T , CM000673.2:g.48212805C>T
GRCh38
NC_000011.9:g.48234357C>T , CM000673.1:g.48234357C>T
GRCh37
NC_000011.8:g.48190933C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'