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Canonical Allele Identifier:
CA13449543
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113408042C>T
GRCh37
chr11:g.113278764C>T
Linked Data - Sequence & Population
gnomAD v2:
11:113278764 C / T
gnomAD v3:
11:113408042 C / T
gnomAD v4:
chr11-113408042-C-T
Joint Max Group AF
0.53461754 (NFE)
Genomes Max Group AF
0.53461754 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1554929
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113408042C>T , CM000673.2:g.113408042C>T
GRCh38
NC_000011.9:g.113278764C>T , CM000673.1:g.113278764C>T
GRCh37
NC_000011.8:g.112783974C>T
NCBI36
NG_008841.1:g.72238G>A
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