ClinGen Allele Registry
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Canonical Allele Identifier:
CA108770427
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.154594243T>G
GRCh37
chr4:g.155515395T>G
Linked Data - Sequence & Population
gnomAD v2:
4:155515395 T / G
gnomAD v3:
4:154594243 T / G
gnomAD v4:
chr4-154594243-T-G
Joint Max Group AF
0.05747739 (AFR)
Genomes Max Group AF
0.05747739 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10050257
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154594243T>G , CM000666.2:g.154594243T>G
GRCh38
NC_000004.11:g.155515395T>G , CM000666.1:g.155515395T>G
GRCh37
NC_000004.10:g.155734845T>G
NCBI36
NG_008832.1:g.1503A>C , LRG_557:g.1503A>C
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