ClinGen Allele Registry
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Canonical Allele Identifier:
CA11757515
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.105127203T>G
GRCh37
chr4:g.106048360T>G
Linked Data - Sequence & Population
gnomAD v2:
4:106048360 T / G
gnomAD v3:
4:105127203 T / G
gnomAD v4:
chr4-105127203-T-G
Joint Max Group AF
0.82451134 (AFR)
Genomes Max Group AF
0.82451134 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1541374
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.105127203T>G , CM000666.2:g.105127203T>G
GRCh38
NC_000004.11:g.106048360T>G , CM000666.1:g.106048360T>G
GRCh37
NC_000004.10:g.106267809T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'