ClinGen Allele Registry
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Canonical Allele Identifier:
CA806247334
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.157603393T>C
GRCh37
chr5:g.157030401T>C
Linked Data - Sequence & Population
gnomAD v3:
5:157603393 T / C
gnomAD v4:
chr5-157603393-T-C
Linked Data - NCBI & NCI
dbSNP:
1373706964
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.157603393T>C , CM000667.2:g.157603393T>C
GRCh38
NC_000005.9:g.157030401T>C , CM000667.1:g.157030401T>C
GRCh37
NC_000005.8:g.156962979T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'