ClinGen Allele Registry
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Canonical Allele Identifier:
CA815487956
Gene:
Linked Data
dbSNP Id:
rs1386940806
MyVariant Identifiers:
chr5:g.91518561C>T (hg19)
chr5:g.92222744C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.92222744C>T , CM000667.2:g.92222744C>T
GRCh38
NC_000005.9:g.91518561C>T , CM000667.1:g.91518561C>T
GRCh37
NC_000005.8:g.91554317C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_948565.1:n.394+18060C>T
Search 100 bp 5'
Search 100 bp 3'