ClinGen Allele Registry
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Canonical Allele Identifier:
CA779336968
Gene:
Linked Data
dbSNP:
2848745
MyVariant.info:
GRCh38
chr18:g.41477761G>A
GRCh37
chr18:g.39057725G>A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.41477761G>A , CM000680.2:g.41477761G>A
GRCh38
NC_000018.9:g.39057725G>A , CM000680.1:g.39057725G>A
GRCh37
NC_000018.8:g.37311723G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_935409.1:n.86-26373G>A
Search 100 bp 5'
Search 100 bp 3'