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Canonical Allele Identifier:
CA11095295
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203878211G>T
GRCh37
chr2:g.204742934G>T
Linked Data - Sequence & Population
gnomAD v2:
2:204742934 G / T
gnomAD v3:
2:203878211 G / T
gnomAD v4:
chr2-203878211-G-T
Joint Max Group AF
0.59686666 (SAS)
Genomes Max Group AF
0.59686666 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11571302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203878211G>T , CM000664.2:g.203878211G>T
GRCh38
NC_000002.11:g.204742934G>T , CM000664.1:g.204742934G>T
GRCh37
NC_000002.10:g.204451179G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'