ClinGen Allele Registry
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Canonical Allele Identifier:
CA585052418
Gene:
Linked Data
dbSNP Id:
rs1306205738
gnomAD v2:
8-128011537-A-T
gnomAD v3:
8-126999292-A-T
gnomAD v4:
8-126999292-A-T
MyVariant Identifiers:
chr8:g.128011537A>T (hg19)
chr8:g.126999292A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.126999292A>T , CM000670.2:g.126999292A>T
GRCh38
NC_000008.10:g.128011537A>T , CM000670.1:g.128011537A>T
GRCh37
NC_000008.9:g.128080719A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746076.2:n.1301-7263A>T
Search 100 bp 5'
Search 100 bp 3'