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Canonical Allele Identifier:
CA16106275
Gene: AFF3
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.100190478T>A
GRCh37
chr2:g.100806940T>A
Linked Data - Sequence & Population
gnomAD v2:
2:100806940 T / A
gnomAD v3:
2:100190478 T / A
gnomAD v4:
chr2-100190478-T-A
Joint Max Group AF
0.59473909 (EAS)
Genomes Max Group AF
0.59473909 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11676922
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.100190478T>A , CM000664.2:g.100190478T>A
GRCh38
NC_000002.11:g.100806940T>A , CM000664.1:g.100806940T>A
GRCh37
NC_000002.10:g.100173372T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000672999.1:n.287+1664A>T
Search 100 bp 5'
Search 100 bp 3'