ClinGen Allele Registry
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Canonical Allele Identifier:
CA847118739
Gene:
Linked Data
dbSNP Id:
rs1240599358
gnomAD v3:
8-127012527-T-C
gnomAD v4:
8-127012527-T-C
MyVariant Identifiers:
chr8:g.128024772T>C (hg19)
chr8:g.127012527T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127012527T>C , CM000670.2:g.127012527T>C
GRCh38
NC_000008.10:g.128024772T>C , CM000670.1:g.128024772T>C
GRCh37
NC_000008.9:g.128093954T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746076.2:n.1364+5909T>C
Search 100 bp 5'
Search 100 bp 3'