ClinGen Allele Registry
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Canonical Allele Identifier:
CA904086766
Gene:
Linked Data
dbSNP Id:
rs1273477778
MyVariant Identifiers:
chr3:g.187649336C>T (hg19)
chr3:g.187931548C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.187931548C>T , CM000665.2:g.187931548C>T
GRCh38
NC_000003.11:g.187649336C>T , CM000665.1:g.187649336C>T
GRCh37
NC_000003.10:g.189132030C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_924814.1:n.1366G>A
Search 100 bp 5'
Search 100 bp 3'