ClinGen Allele Registry
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Canonical Allele Identifier:
CA11702483
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.140569265T>G
GRCh37
chr4:g.141490419T>G
Linked Data - Sequence & Population
gnomAD v2:
4:141490419 T / G
gnomAD v3:
4:140569265 T / G
gnomAD v4:
chr4-140569265-T-G
Joint Max Group AF
0.6032226 (AFR)
Genomes Max Group AF
0.6032226 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3811787
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.140569265T>G , CM000666.2:g.140569265T>G
GRCh38
NC_000004.11:g.141490419T>G , CM000666.1:g.141490419T>G
GRCh37
NC_000004.10:g.141709869T>G
NCBI36
NG_012139.1:g.4541A>C
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