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Canonical Allele Identifier:
CA31393702
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159724419G>T
GRCh37
chr1:g.159694209G>T
Linked Data - Sequence & Population
gnomAD v2:
1:159694209 G / T
gnomAD v3:
1:159724419 G / T
gnomAD v4:
chr1-159724419-G-T
Joint Max Group AF
0.80414213 (EAS)
Genomes Max Group AF
0.80414213 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2808635
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159724419G>T , CM000663.2:g.159724419G>T
GRCh38
NC_000001.10:g.159694209G>T , CM000663.1:g.159694209G>T
GRCh37
NC_000001.9:g.157960833G>T
NCBI36
Search 100 bp 5'
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