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Canonical Allele Identifier:
CA15409629
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.153488877T>C
GRCh37
chr5:g.152868437T>C
Linked Data - Sequence & Population
gnomAD v2:
5:152868437 T / C
gnomAD v3:
5:153488877 T / C
gnomAD v4:
chr5-153488877-T-C
Joint Max Group AF
0.70186982 (EAS)
Genomes Max Group AF
0.70186982 (EAS)
Linked Data - NCBI & NCI
dbSNP:
548294
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.153488877T>C , CM000667.2:g.153488877T>C
GRCh38
NC_000005.9:g.152868437T>C , CM000667.1:g.152868437T>C
GRCh37
NC_000005.8:g.152848630T>C
NCBI36
NG_047078.1:g.4182T>C
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