Linked Data
dbSNP Id:
rs9512900
gnomAD v2:
13-28429738-T-C
gnomAD v3:
13-27855601-T-C
gnomAD v4:
13-27855601-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27855601T>C , CM000675.2:g.27855601T>C | GRCh38 |
| NC_000013.10:g.28429738T>C , CM000675.1:g.28429738T>C | GRCh37 |
| NC_000013.9:g.27327738T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_047484.1:n.242-7065A>G | ||
| NR_047484.2:n.143-7065A>G |