ClinGen Allele Registry
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Canonical Allele Identifier:
CA699139581
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.54179837T>G
GRCh37
chr13:g.54753972T>G
Linked Data - Sequence & Population
gnomAD v3:
13:54179837 T / G
gnomAD v4:
chr13-54179837-T-G
Linked Data - NCBI & NCI
dbSNP:
795659
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.54179837T>G , CM000675.2:g.54179837T>G
GRCh38
NC_000013.10:g.54753972T>G , CM000675.1:g.54753972T>G
GRCh37
NC_000013.9:g.53651973T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'