ClinGen Allele Registry
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Canonical Allele Identifier:
CA899525139
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.137728643G>T
GRCh37
chr3:g.137447485G>T
Linked Data - Sequence & Population
gnomAD v3:
3:137728643 G / T
gnomAD v4:
chr3-137728643-G-T
Linked Data - NCBI & NCI
dbSNP:
10935268
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.137728643G>T , CM000665.2:g.137728643G>T
GRCh38
NC_000003.11:g.137447485G>T , CM000665.1:g.137447485G>T
GRCh37
NC_000003.10:g.138930175G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'