Canonical Allele Identifier: CA16216483
Gene:
MyVariant.info:
GRCh38 chr5:g.1308437G>A
GRCh37 chr5:g.1308552G>A
gnomAD v2:
5:1308552 G / A
gnomAD v3:
5:1308437 G / A
gnomAD v4:
chr5-1308437-G-A
Joint Max Group AF 0.3143345 (AFR)
Genomes Max Group AF 0.3143345 (AFR)
dbSNP:
4635969
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1308437G>A , CM000667.2:g.1308437G>A GRCh38
NC_000005.9:g.1308552G>A , CM000667.1:g.1308552G>A GRCh37
NC_000005.8:g.1361552G>A NCBI36
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