Linked Data
dbSNP Id:
rs933100654
gnomAD v4:
13-48303670-A-G
MyVariant Identifiers:
chr13:g.48303670A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303670A>G , CM000675.2:g.48303670A>G | GRCh38 |
| NC_000013.10:g.48877806A>G , CM000675.1:g.48877806A>G | GRCh37 |
| NC_000013.9:g.47775807A>G | NCBI36 |
| NG_009009.1:g.4924A>G , LRG_517:g.4924A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046414.2:n.33T>C |