ClinGen Allele Registry
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Canonical Allele Identifier:
CA12109900
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.175439088T>G
GRCh37
chr5:g.174866091T>G
Linked Data - Sequence & Population
gnomAD v2:
5:174866091 T / G
gnomAD v3:
5:175439088 T / G
gnomAD v4:
chr5-175439088-T-G
Joint Max Group AF
0.23334726 (MID)
Genomes Max Group AF
0.20886039 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11746641
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.175439088T>G , CM000667.2:g.175439088T>G
GRCh38
NC_000005.9:g.174866091T>G , CM000667.1:g.174866091T>G
GRCh37
NC_000005.8:g.174798697T>G
NCBI36
NG_011802.1:g.10073A>C
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