ClinGen Allele Registry
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Canonical Allele Identifier:
CA811014396
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.44691293T>A
GRCh37
chr5:g.44691395T>A
Linked Data - Sequence & Population
gnomAD v3:
5:44691293 T / A
gnomAD v4:
chr5-44691293-T-A
Linked Data - NCBI & NCI
dbSNP:
6451770
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.44691293T>A , CM000667.2:g.44691293T>A
GRCh38
NC_000005.9:g.44691395T>A , CM000667.1:g.44691395T>A
GRCh37
NC_000005.8:g.44727152T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'