ClinGen Allele Registry
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Canonical Allele Identifier:
CA130189239
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.157603237G>A
GRCh37
chr5:g.157030245G>A
Linked Data - Sequence & Population
gnomAD v3:
5:157603237 G / A
Linked Data - NCBI & NCI
dbSNP:
181381079
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.157603237G>A , CM000667.2:g.157603237G>A
GRCh38
NC_000005.9:g.157030245G>A , CM000667.1:g.157030245G>A
GRCh37
NC_000005.8:g.156962823G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'