ClinGen Allele Registry
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Canonical Allele Identifier:
CA11989658
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.173236451C>T
GRCh37
chr5:g.172663454C>T
Linked Data - Sequence & Population
gnomAD v2:
5:172663454 C / T
gnomAD v3:
5:173236451 C / T
gnomAD v4:
chr5-173236451-C-T
Joint Max Group AF
0.36030491 (SAS)
Genomes Max Group AF
0.36030491 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3095870
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.173236451C>T , CM000667.2:g.173236451C>T
GRCh38
NC_000005.9:g.172663454C>T , CM000667.1:g.172663454C>T
GRCh37
NC_000005.8:g.172596060C>T
NCBI36
NG_013340.1:g.3862G>A
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