Canonical Allele Identifier:
CA14703614
Gene:
Linked Data
ClinVar Variation Id:
619951
ClinVar RCV Id:
RCV000845578
dbSNP Id:
rs405509
gnomAD v2:
19-45408836-T-G
gnomAD v3:
19-44905579-T-G
gnomAD v4:
19-44905579-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44905579T>G , CM000681.2:g.44905579T>G | GRCh38 |
| NC_000019.9:g.45408836T>G , CM000681.1:g.45408836T>G | GRCh37 |
| NC_000019.8:g.50100676T>G | NCBI36 |
| NG_007084.2:g.4798T>G | |
| NG_042854.1:g.19360T>G |