ClinGen Allele Registry
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Canonical Allele Identifier:
CA129850805
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.159387413G>A
GRCh37
chr5:g.158814421G>A
Linked Data - NCBI & NCI
dbSNP:
777120277
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.159387413G>A , CM000667.2:g.159387413G>A
GRCh38
NC_000005.9:g.158814421G>A , CM000667.1:g.158814421G>A
GRCh37
NC_000005.8:g.158746999G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'