ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA778454247
Gene:
Linked Data
dbSNP Id:
rs1438560602
gnomAD v3:
18-31756780-A-G
gnomAD v4:
18-31756780-A-G
MyVariant Identifiers:
chr18:g.29336743A>G (hg19)
chr18:g.31756780A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.31756780A>G , CM000680.2:g.31756780A>G
GRCh38
NC_000018.9:g.29336743A>G , CM000680.1:g.29336743A>G
GRCh37
NC_000018.8:g.27590741A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_935338.1:n.66-5359A>G
Search 100 bp 5'
Search 100 bp 3'