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Canonical Allele Identifier:
CA31391218
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159715192T>C
GRCh37
chr1:g.159684982T>C
Linked Data - Sequence & Population
gnomAD v2:
1:159684982 T / C
gnomAD v3:
1:159715192 T / C
gnomAD v4:
chr1-159715192-T-C
Joint Max Group AF
0.15516651 (AFR)
Genomes Max Group AF
0.15516651 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3093061
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159715192T>C , CM000663.2:g.159715192T>C
GRCh38
NC_000001.10:g.159684982T>C , CM000663.1:g.159684982T>C
GRCh37
NC_000001.9:g.157951606T>C
NCBI36
NG_013007.1:g.4398A>G
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