ClinGen Allele Registry
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Canonical Allele Identifier:
CA619976110
Gene:
Linked Data
dbSNP Id:
rs1316837980
gnomAD v2:
15-96325593-A-G
gnomAD v3:
15-95782364-A-G
gnomAD v4:
15-95782364-A-G
MyVariant Identifiers:
chr15:g.96325593A>G (hg19)
chr15:g.95782364A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.95782364A>G , CM000677.2:g.95782364A>G
GRCh38
NC_000015.9:g.96325593A>G , CM000677.1:g.96325593A>G
GRCh37
NC_000015.8:g.94126597A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_932654.1:n.148-42825A>G
Search 100 bp 5'
Search 100 bp 3'