ClinGen Allele Registry
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Canonical Allele Identifier:
CA779336971
Gene:
Linked Data
dbSNP Id:
rs750850446
gnomAD v3:
18-41477762-G-T
gnomAD v4:
18-41477762-G-T
MyVariant Identifiers:
chr18:g.39057726G>T (hg19)
chr18:g.41477762G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.41477762G>T , CM000680.2:g.41477762G>T
GRCh38
NC_000018.9:g.39057726G>T , CM000680.1:g.39057726G>T
GRCh37
NC_000018.8:g.37311724G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_935409.1:n.86-26372G>T
Search 100 bp 5'
Search 100 bp 3'